Canonical Allele Identifier: CA1857429082

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794186T= , CM000671.2:g.77794186T=	GRCh38
NC_000009.11:g.80409102T= , CM000671.1:g.80409102T=	GRCh37
NC_000009.10:g.79598922T=	NCBI36
NG_027904.2:g.242118A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+277A= MANE Select	ENSP00000286548.4:n.735+277A=
ENST00000286548.8:c.735+277A=	ENSP00000286548.4:n.735+277A=
NM_002072.4:c.735+277A=	NP_002063.2:n.735+277A=
XM_017014628.2:c.561+277A=	XP_016870117.1:n.561+277A=
NM_002072.5:c.735+277A= MANE Select	NP_002063.2:n.735+277A=