Canonical Allele Identifier: CA465578320
Gene: GNAQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80409442G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794526G>C , CM000671.2:g.77794526G>C GRCh38
NC_000009.11:g.80409442G>C , CM000671.1:g.80409442G>C GRCh37
NC_000009.10:g.79599262G>C NCBI36
NG_027904.2:g.241778C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.672C>G MANE Select ENSP00000286548.4:p.Thr224=
ENST00000286548.8:c.672C>G ENSP00000286548.4:p.Thr224=
NM_002072.4:c.672C>G NP_002063.2:p.Thr224=
XM_017014628.2:c.498C>G XP_016870117.1:p.Thr166=
NM_002072.5:c.672C>G MANE Select NP_002063.2:p.Thr224=
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