Canonical Allele Identifier: CA373997701
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118443286
MyVariant Identifiers: chr9:g.80409411A>C (hg19) chr9:g.77794495A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794495A>C , CM000671.2:g.77794495A>C GRCh38
NC_000009.11:g.80409411A>C , CM000671.1:g.80409411A>C GRCh37
NC_000009.10:g.79599231A>C NCBI36
NG_027904.2:g.241809T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.703T>G MANE Select ENSP00000286548.4:p.Tyr235Asp
ENST00000286548.8:c.703T>G ENSP00000286548.4:p.Tyr235Asp
NM_002072.4:c.703T>G NP_002063.2:p.Tyr235Asp
XM_017014628.2:c.529T>G XP_016870117.1:p.Tyr177Asp
NM_002072.5:c.703T>G MANE Select NP_002063.2:p.Tyr235Asp
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