Canonical Allele Identifier: CA373997913
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444534

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.613G>T MANE Select ENSP00000286548.4:p.Asp205Tyr
ENST00000286548.8:c.613G>T ENSP00000286548.4:p.Asp205Tyr
NM_002072.4:c.613G>T NP_002063.2:p.Asp205Tyr
XM_017014628.2:c.439G>T XP_016870117.1:p.Asp147Tyr
NM_002072.5:c.613G>T MANE Select NP_002063.2:p.Asp205Tyr