Canonical Allele Identifier: CA424733820
Gene: OR13G1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.247835963A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672661A>T , CM000663.2:g.247672661A>T GRCh38
NC_000001.10:g.247835963A>T , CM000663.1:g.247835963A>T GRCh37
NC_000001.9:g.245902586A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.381T>A ENSP00000352717.2:p.Leu127=
ENST00000642119.1:c.381T>A MANE Select ENSP00000493110.1:p.Leu127=
ENST00000359688.3:c.381T>A ENSP00000352717.2:p.Leu127=
NM_001005487.1:c.381T>A NP_001005487.1:p.Leu127=
NM_001005487.2:c.381T>A MANE Select NP_001005487.1:p.Leu127=
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