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 7:30976439 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020716

Most severe consequence
Clinical significance

Synonyms

LSDB 2346

This variation has 13 HGVS names - click the plus to show

7:g.30976439A>G
ENST00000409904.5:c.793A>G
ENSP00000387113.3:p.Lys265Glu
ENST00000337750.7:c.*201A>G
ENST00000463164.1:n.11A>G
ENST00000409316.3:c.284A>G
ENSP00000386602.1:p.Gln95Arg
ENST00000611037.1:c.431A>G
ENSP00000480159.1:p.Gln144Arg
ENST00000396227.4:c.*201A>G
ENST00000461424.3:n.561A>G
ENST00000326139.4:c.985A>G
ENSP00000320180.2:p.Lys329Glu

Variation displays