Canonical Allele Identifier: CA373997887
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118444382
gnomAD v4: 9-77794573-G-T
COSMIC: COSM132932

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.625C>A MANE Select ENSP00000286548.4:p.Gln209Lys
ENST00000286548.8:c.625C>A ENSP00000286548.4:p.Gln209Lys
NM_002072.4:c.625C>A NP_002063.2:p.Gln209Lys
XM_017014628.2:c.451C>A XP_016870117.1:p.Gln151Lys
NM_002072.5:c.625C>A MANE Select NP_002063.2:p.Gln209Lys