Canonical Allele Identifier: CA2690385215

Gene: GNAQ

Linked Data

• gnomAD v4: 9-77794668-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794668A>C , CM000671.2:g.77794668A>C	GRCh38
NC_000009.11:g.80409584A>C , CM000671.1:g.80409584A>C	GRCh37
NC_000009.10:g.79599404A>C	NCBI36
NG_027904.2:g.241636T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-76T>G MANE Select	ENSP00000286548.4:n.606-76T>G
ENST00000286548.8:c.606-76T>G	ENSP00000286548.4:n.606-76T>G
NM_002072.4:c.606-76T>G	NP_002063.2:n.606-76T>G
XM_017014628.2:c.432-76T>G	XP_016870117.1:n.432-76T>G
NM_002072.5:c.606-76T>G MANE Select	NP_002063.2:n.606-76T>G