Canonical Allele Identifier: CA2555288941

Gene: GNAQ

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794165A>G , CM000671.2:g.77794165A>G	GRCh38
NC_000009.11:g.80409081A>G , CM000671.1:g.80409081A>G	GRCh37
NC_000009.10:g.79598901A>G	NCBI36
NG_027904.2:g.242139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+298T>C MANE Select	ENSP00000286548.4:n.735+298T>C
ENST00000286548.8:c.735+298T>C	ENSP00000286548.4:n.735+298T>C
NM_002072.4:c.735+298T>C	NP_002063.2:n.735+298T>C
XM_017014628.2:c.561+298T>C	XP_016870117.1:n.561+298T>C
NM_002072.5:c.735+298T>C MANE Select	NP_002063.2:n.735+298T>C