Canonical Allele Identifier: CA2719859326

Gene: GNAQ

Linked Data

• dbSNP Id: rs2118444845

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794623C>A , CM000671.2:g.77794623C>A	GRCh38
NC_000009.11:g.80409539C>A , CM000671.1:g.80409539C>A	GRCh37
NC_000009.10:g.79599359C>A	NCBI36
NG_027904.2:g.241681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.606-31G>T MANE Select	ENSP00000286548.4:n.606-31G>T
ENST00000286548.8:c.606-31G>T	ENSP00000286548.4:n.606-31G>T
NM_002072.4:c.606-31G>T	NP_002063.2:n.606-31G>T
XM_017014628.2:c.432-31G>T	XP_016870117.1:n.432-31G>T
NM_002072.5:c.606-31G>T MANE Select	NP_002063.2:n.606-31G>T