Canonical Allele Identifier: CA9174491
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs774392604
ExAC: 19:9236959 G / T
gnomAD v2: 19-9236959-G-T
gnomAD v3: 19-9126283-G-T
gnomAD v4: 19-9126283-G-T
MyVariant Identifiers: chr19:g.9236959G>T (hg19) chr19:g.9126283G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126283G>T , CM000681.2:g.9126283G>T GRCh38
NC_000019.9:g.9236959G>T , CM000681.1:g.9236959G>T GRCh37
NC_000019.8:g.9097959G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.668C>A MANE Select ENSP00000302867.2:p.Ser223Tyr
NM_001001958.1:c.668C>A MANE Select NP_001001958.1:p.Ser223Tyr
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