Canonical Allele Identifier: CA9174529
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs147006672
ExAC: 19:9237113 G / C
gnomAD v2: 19-9237113-G-C
gnomAD v3: 19-9126437-G-C
gnomAD v4: 19-9126437-G-C
MyVariant Identifiers: chr19:g.9237113G>C (hg19) chr19:g.9126437G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126437G>C , CM000681.2:g.9126437G>C GRCh38
NC_000019.9:g.9237113G>C , CM000681.1:g.9237113G>C GRCh37
NC_000019.8:g.9098113G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.514C>G MANE Select ENSP00000302867.2:p.Leu172Val
NM_001001958.1:c.514C>G MANE Select NP_001001958.1:p.Leu172Val
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