Canonical Allele Identifier: CA9174490
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs771183236
ExAC: 19:9236958 G / T
gnomAD v2: 19-9236958-G-T
gnomAD v4: 19-9126282-G-T
MyVariant Identifiers: chr19:g.9236958G>T (hg19) chr19:g.9126282G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126282G>T , CM000681.2:g.9126282G>T GRCh38
NC_000019.9:g.9236958G>T , CM000681.1:g.9236958G>T GRCh37
NC_000019.8:g.9097958G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.669C>A MANE Select ENSP00000302867.2:p.Ser223=
NM_001001958.1:c.669C>A MANE Select NP_001001958.1:p.Ser223=
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