Canonical Allele Identifier: CA1857429059

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794157G= , CM000671.2:g.77794157G=	GRCh38
NC_000009.11:g.80409073G= , CM000671.1:g.80409073G=	GRCh37
NC_000009.10:g.79598893G=	NCBI36
NG_027904.2:g.242147C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+306C= MANE Select	ENSP00000286548.4:n.735+306C=
ENST00000286548.8:c.735+306C=	ENSP00000286548.4:n.735+306C=
NM_002072.4:c.735+306C=	NP_002063.2:n.735+306C=
XM_017014628.2:c.561+306C=	XP_016870117.1:n.561+306C=
NM_002072.5:c.735+306C= MANE Select	NP_002063.2:n.735+306C=