Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 17:81510709 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM063834

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_008_ACTG1_102560_0006

This variation has 16 HGVS names - click the plus to show

17:g.81510709A>G
ENST00000576209.3:n.994T>C
ENST00000576917.3:n.1241T>C
ENST00000575842.3:c.1109T>C
ENSP00000458162.1:p.Val370Ala
ENST00000615544.2:c.1109T>C
ENSP00000477968.1:p.Val370Ala
ENST00000573283.3:c.1109T>C
ENSP00000458435.1:p.Val370Ala
ENST00000331925.4:c.1109T>C
ENSP00000331514.2:p.Val370Ala
ENST00000574671.3:n.968T>C
ENST00000575087.3:c.1109T>C
ENSP00000459124.1:p.Val370Ala
ENST00000576544.3:c.1109T>C
ENSP00000461672.1:p.Val370Ala

Variation displays