Canonical Allele Identifier: CA194717229

Gene: GNAQ

Linked Data

• dbSNP Id: rs908093330
• MyVariant Identifiers: chr9:g.80409096G>A (hg19) ; chr9:g.77794180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.77794180G>A , CM000671.2:g.77794180G>A	GRCh38
NC_000009.11:g.80409096G>A , CM000671.1:g.80409096G>A	GRCh37
NC_000009.10:g.79598916G>A	NCBI36
NG_027904.2:g.242124C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286548.9:c.735+283C>T MANE Select	ENSP00000286548.4:n.735+283C>T
ENST00000286548.8:c.735+283C>T	ENSP00000286548.4:n.735+283C>T
NM_002072.4:c.735+283C>T	NP_002063.2:n.735+283C>T
XM_017014628.2:c.561+283C>T	XP_016870117.1:n.561+283C>T
NM_002072.5:c.735+283C>T MANE Select	NP_002063.2:n.735+283C>T