Canonical Allele Identifier: CA373997863

Gene: GNAQ

Linked Data

• MyVariant Identifiers: chr9:g.80409478C>G (hg19) ; chr9:g.77794562C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794562C>G , CM000671.2:g.77794562C>G	GRCh38
NC_000009.11:g.80409478C>G , CM000671.1:g.80409478C>G	GRCh37
NC_000009.10:g.79599298C>G	NCBI36
NG_027904.2:g.241742G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.636G>C MANE Select	ENSP00000286548.4:p.Glu212Asp
ENST00000286548.8:c.636G>C	ENSP00000286548.4:p.Glu212Asp
NM_002072.4:c.636G>C	NP_002063.2:p.Glu212Asp
XM_017014628.2:c.462G>C	XP_016870117.1:p.Glu154Asp
NM_002072.5:c.636G>C MANE Select	NP_002063.2:p.Glu212Asp