Canonical Allele Identifier: CA373997917
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444556
MyVariant Identifiers: chr9:g.80409504C>A (hg19) chr9:g.77794588C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794588C>A , CM000671.2:g.77794588C>A GRCh38
NC_000009.11:g.80409504C>A , CM000671.1:g.80409504C>A GRCh37
NC_000009.10:g.79599324C>A NCBI36
NG_027904.2:g.241716G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.610G>T MANE Select ENSP00000286548.4:p.Val204Phe
ENST00000286548.8:c.610G>T ENSP00000286548.4:p.Val204Phe
NM_002072.4:c.610G>T NP_002063.2:p.Val204Phe
XM_017014628.2:c.436G>T XP_016870117.1:p.Val146Phe
NM_002072.5:c.610G>T MANE Select NP_002063.2:p.Val204Phe
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