Canonical Allele Identifier: CA373997657
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794476T>A , CM000671.2:g.77794476T>A GRCh38
NC_000009.11:g.80409392T>A , CM000671.1:g.80409392T>A GRCh37
NC_000009.10:g.79599212T>A NCBI36
NG_027904.2:g.241828A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.722A>T MANE Select ENSP00000286548.4:p.Glu241Val
ENST00000286548.8:c.722A>T ENSP00000286548.4:p.Glu241Val
NM_002072.4:c.722A>T NP_002063.2:p.Glu241Val
XM_017014628.2:c.548A>T XP_016870117.1:p.Glu183Val
NM_002072.5:c.722A>T MANE Select NP_002063.2:p.Glu241Val