Canonical Allele Identifier: CA505452820
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1310791762
gnomAD v4: 19-9126510-C-T
MyVariant Identifiers: chr19:g.9237186C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126510C>T , CM000681.2:g.9126510C>T GRCh38
NC_000019.9:g.9237186C>T , CM000681.1:g.9237186C>T GRCh37
NC_000019.8:g.9098186C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.441G>A MANE Select ENSP00000302867.2:p.Leu147=
NM_001001958.1:c.441G>A MANE Select NP_001001958.1:p.Leu147=
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