Canonical Allele Identifier: CA1857429035

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794113C= , CM000671.2:g.77794113C=	GRCh38
NC_000009.11:g.80409029C= , CM000671.1:g.80409029C=	GRCh37
NC_000009.10:g.79598849C=	NCBI36
NG_027904.2:g.242191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+350G= MANE Select	ENSP00000286548.4:n.735+350G=
ENST00000286548.8:c.735+350G=	ENSP00000286548.4:n.735+350G=
NM_002072.4:c.735+350G=	NP_002063.2:n.735+350G=
XM_017014628.2:c.561+350G=	XP_016870117.1:n.561+350G=
NM_002072.5:c.735+350G= MANE Select	NP_002063.2:n.735+350G=