Canonical Allele Identifier: CA373997771
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118443735
MyVariant Identifiers: chr9:g.80409441A>T (hg19) chr9:g.77794525A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794525A>T , CM000671.2:g.77794525A>T GRCh38
NC_000009.11:g.80409441A>T , CM000671.1:g.80409441A>T GRCh37
NC_000009.10:g.79599261A>T NCBI36
NG_027904.2:g.241779T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.673T>A MANE Select ENSP00000286548.4:p.Ser225Thr
ENST00000286548.8:c.673T>A ENSP00000286548.4:p.Ser225Thr
NM_002072.4:c.673T>A NP_002063.2:p.Ser225Thr
XM_017014628.2:c.499T>A XP_016870117.1:p.Ser167Thr
NM_002072.5:c.673T>A MANE Select NP_002063.2:p.Ser225Thr
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