Canonical Allele Identifier: CA373997889
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444392

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794575C>G , CM000671.2:g.77794575C>G GRCh38
NC_000009.11:g.80409491C>G , CM000671.1:g.80409491C>G GRCh37
NC_000009.10:g.79599311C>G NCBI36
NG_027904.2:g.241729G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.623G>C MANE Select ENSP00000286548.4:p.Gly208Ala
ENST00000286548.8:c.623G>C ENSP00000286548.4:p.Gly208Ala
NM_002072.4:c.623G>C NP_002063.2:p.Gly208Ala
XM_017014628.2:c.449G>C XP_016870117.1:p.Gly150Ala
NM_002072.5:c.623G>C MANE Select NP_002063.2:p.Gly208Ala