Canonical Allele Identifier: CA373997911
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444534

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794585C>G , CM000671.2:g.77794585C>G GRCh38
NC_000009.11:g.80409501C>G , CM000671.1:g.80409501C>G GRCh37
NC_000009.10:g.79599321C>G NCBI36
NG_027904.2:g.241719G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.613G>C MANE Select ENSP00000286548.4:p.Asp205His
ENST00000286548.8:c.613G>C ENSP00000286548.4:p.Asp205His
NM_002072.4:c.613G>C NP_002063.2:p.Asp205His
XM_017014628.2:c.439G>C XP_016870117.1:p.Asp147His
NM_002072.5:c.613G>C MANE Select NP_002063.2:p.Asp205His