Canonical Allele Identifier: CA373997898
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794579C>T , CM000671.2:g.77794579C>T GRCh38
NC_000009.11:g.80409495C>T , CM000671.1:g.80409495C>T GRCh37
NC_000009.10:g.79599315C>T NCBI36
NG_027904.2:g.241725G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.619G>A MANE Select ENSP00000286548.4:p.Gly207Arg
ENST00000286548.8:c.619G>A ENSP00000286548.4:p.Gly207Arg
NM_002072.4:c.619G>A NP_002063.2:p.Gly207Arg
XM_017014628.2:c.445G>A XP_016870117.1:p.Gly149Arg
NM_002072.5:c.619G>A MANE Select NP_002063.2:p.Gly207Arg