Canonical Allele Identifier: CA9174494
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs775795889
ExAC: 19:9236965 A / G
gnomAD v2: 19-9236965-A-G
gnomAD v3: 19-9126289-A-G
gnomAD v4: 19-9126289-A-G
MyVariant Identifiers: chr19:g.9236965A>G (hg19) chr19:g.9126289A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126289A>G , CM000681.2:g.9126289A>G GRCh38
NC_000019.9:g.9236965A>G , CM000681.1:g.9236965A>G GRCh37
NC_000019.8:g.9097965A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.662T>C MANE Select ENSP00000302867.2:p.Ile221Thr
NM_001001958.1:c.662T>C MANE Select NP_001001958.1:p.Ile221Thr
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