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 11:17387652 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960894

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

11:g.17387652A>G
ENST00000528992.1:c.457T>C
ENSP00000436479.1:p.Leu153Pro
ENST00000526912.1:c.179T>C
ENSP00000432729.1:p.Leu60Pro
ENST00000528731.1:c.179T>C
ENSP00000434755.1:p.Leu60Pro
ENST00000339994.4:c.440T>C
ENSP00000345708.4:p.Leu147Pro

Variation displays