Canonical Allele Identifier: CA2690385068

Gene: GNAQ

Linked Data

• gnomAD v4: 9-77794399-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794399T>C , CM000671.2:g.77794399T>C	GRCh38
NC_000009.11:g.80409315T>C , CM000671.1:g.80409315T>C	GRCh37
NC_000009.10:g.79599135T>C	NCBI36
NG_027904.2:g.241905A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+64A>G MANE Select	ENSP00000286548.4:n.735+64A>G
ENST00000286548.8:c.735+64A>G	ENSP00000286548.4:n.735+64A>G
NM_002072.4:c.735+64A>G	NP_002063.2:n.735+64A>G
XM_017014628.2:c.561+64A>G	XP_016870117.1:n.561+64A>G
NM_002072.5:c.735+64A>G MANE Select	NP_002063.2:n.735+64A>G