Canonical Allele Identifier: CA373997901

Gene: GNAQ

Linked Data

• MyVariant Identifiers: chr9:g.80409497A>G (hg19) ; chr9:g.77794581A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794581A>G , CM000671.2:g.77794581A>G	GRCh38
NC_000009.11:g.80409497A>G , CM000671.1:g.80409497A>G	GRCh37
NC_000009.10:g.79599317A>G	NCBI36
NG_027904.2:g.241723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.617T>C MANE Select	ENSP00000286548.4:p.Val206Ala
ENST00000286548.8:c.617T>C	ENSP00000286548.4:p.Val206Ala
NM_002072.4:c.617T>C	NP_002063.2:p.Val206Ala
XM_017014628.2:c.443T>C	XP_016870117.1:p.Val148Ala
NM_002072.5:c.617T>C MANE Select	NP_002063.2:p.Val206Ala