Canonical Allele Identifier: CA1857429080

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794182T= , CM000671.2:g.77794182T=	GRCh38
NC_000009.11:g.80409098T= , CM000671.1:g.80409098T=	GRCh37
NC_000009.10:g.79598918T=	NCBI36
NG_027904.2:g.242122A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+281A= MANE Select	ENSP00000286548.4:n.735+281A=
ENST00000286548.8:c.735+281A=	ENSP00000286548.4:n.735+281A=
NM_002072.4:c.735+281A=	NP_002063.2:n.735+281A=
XM_017014628.2:c.561+281A=	XP_016870117.1:n.561+281A=
NM_002072.5:c.735+281A= MANE Select	NP_002063.2:n.735+281A=