Canonical Allele Identifier: CA465578287
Gene: GNAQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80409388T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794472T>A , CM000671.2:g.77794472T>A GRCh38
NC_000009.11:g.80409388T>A , CM000671.1:g.80409388T>A GRCh37
NC_000009.10:g.79599208T>A NCBI36
NG_027904.2:g.241832A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.726A>T MANE Select ENSP00000286548.4:p.Ser242=
ENST00000286548.8:c.726A>T ENSP00000286548.4:p.Ser242=
NM_002072.4:c.726A>T NP_002063.2:p.Ser242=
XM_017014628.2:c.552A>T XP_016870117.1:p.Ser184=
NM_002072.5:c.726A>T MANE Select NP_002063.2:p.Ser242=