Canonical Allele Identifier: CA465578332
Gene: GNAQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80409475T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794559T>C , CM000671.2:g.77794559T>C GRCh38
NC_000009.11:g.80409475T>C , CM000671.1:g.80409475T>C GRCh37
NC_000009.10:g.79599295T>C NCBI36
NG_027904.2:g.241745A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.639A>G MANE Select ENSP00000286548.4:p.Arg213=
ENST00000286548.8:c.639A>G ENSP00000286548.4:p.Arg213=
NM_002072.4:c.639A>G NP_002063.2:p.Arg213=
XM_017014628.2:c.465A>G XP_016870117.1:p.Arg155=
NM_002072.5:c.639A>G MANE Select NP_002063.2:p.Arg213=
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