Canonical Allele Identifier: CA373997663
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118442986

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794479A>C , CM000671.2:g.77794479A>C GRCh38
NC_000009.11:g.80409395A>C , CM000671.1:g.80409395A>C GRCh37
NC_000009.10:g.79599215A>C NCBI36
NG_027904.2:g.241825T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.719T>G MANE Select ENSP00000286548.4:p.Val240Gly
ENST00000286548.8:c.719T>G ENSP00000286548.4:p.Val240Gly
NM_002072.4:c.719T>G NP_002063.2:p.Val240Gly
XM_017014628.2:c.545T>G XP_016870117.1:p.Val182Gly
NM_002072.5:c.719T>G MANE Select NP_002063.2:p.Val240Gly