Canonical Allele Identifier: CA373997886
Gene: GNAQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794573G>C , CM000671.2:g.77794573G>C GRCh38
NC_000009.11:g.80409489G>C , CM000671.1:g.80409489G>C GRCh37
NC_000009.10:g.79599309G>C NCBI36
NG_027904.2:g.241731C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.625C>G MANE Select ENSP00000286548.4:p.Gln209Glu
ENST00000286548.8:c.625C>G ENSP00000286548.4:p.Gln209Glu
NM_002072.4:c.625C>G NP_002063.2:p.Gln209Glu
XM_017014628.2:c.451C>G XP_016870117.1:p.Gln151Glu
NM_002072.5:c.625C>G MANE Select NP_002063.2:p.Gln209Glu