Canonical Allele Identifier: CA1857429488

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794613A= , CM000671.2:g.77794613A=	GRCh38
NC_000009.11:g.80409529A= , CM000671.1:g.80409529A=	GRCh37
NC_000009.10:g.79599349A=	NCBI36
NG_027904.2:g.241691T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-21T= MANE Select	ENSP00000286548.4:n.606-21T=
ENST00000286548.8:c.606-21T=	ENSP00000286548.4:n.606-21T=
NM_002072.4:c.606-21T=	NP_002063.2:n.606-21T=
XM_017014628.2:c.432-21T=	XP_016870117.1:n.432-21T=
NM_002072.5:c.606-21T= MANE Select	NP_002063.2:n.606-21T=