Canonical Allele Identifier: CA373997686
Gene: GNAQ HGNC NCBI

Linked Data

dbSNP Id: rs2118443190
MyVariant Identifiers: chr9:g.80409405G>C (hg19) chr9:g.77794489G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77794489G>C , CM000671.2:g.77794489G>C GRCh38
NC_000009.11:g.80409405G>C , CM000671.1:g.80409405G>C GRCh37
NC_000009.10:g.79599225G>C NCBI36
NG_027904.2:g.241815C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286548.9:c.709C>G MANE Select ENSP00000286548.4:p.Gln237Glu
ENST00000286548.8:c.709C>G ENSP00000286548.4:p.Gln237Glu
NM_002072.4:c.709C>G NP_002063.2:p.Gln237Glu
XM_017014628.2:c.535C>G XP_016870117.1:p.Gln179Glu
NM_002072.5:c.709C>G MANE Select NP_002063.2:p.Gln237Glu
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Search 100 bp 3'