Canonical Allele Identifier: CA465578290
Gene: GNAQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80409391C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794475C>T , CM000671.2:g.77794475C>T GRCh38
NC_000009.11:g.80409391C>T , CM000671.1:g.80409391C>T GRCh37
NC_000009.10:g.79599211C>T NCBI36
NG_027904.2:g.241829G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286548.9:c.723G>A MANE Select ENSP00000286548.4:p.Glu241=
ENST00000286548.8:c.723G>A ENSP00000286548.4:p.Glu241=
NM_002072.4:c.723G>A NP_002063.2:p.Glu241=
XM_017014628.2:c.549G>A XP_016870117.1:p.Glu183=
NM_002072.5:c.723G>A MANE Select NP_002063.2:p.Glu241=