Canonical Allele Identifier: CA373997778

Gene: GNAQ

Linked Data

• MyVariant Identifiers: chr9:g.80409446A>C (hg19) ; chr9:g.77794530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794530A>C , CM000671.2:g.77794530A>C	GRCh38
NC_000009.11:g.80409446A>C , CM000671.1:g.80409446A>C	GRCh37
NC_000009.10:g.79599266A>C	NCBI36
NG_027904.2:g.241774T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.668T>G MANE Select	ENSP00000286548.4:p.Val223Gly
ENST00000286548.8:c.668T>G	ENSP00000286548.4:p.Val223Gly
NM_002072.4:c.668T>G	NP_002063.2:p.Val223Gly
XM_017014628.2:c.494T>G	XP_016870117.1:p.Val165Gly
NM_002072.5:c.668T>G MANE Select	NP_002063.2:p.Val223Gly