Canonical Allele Identifier: CA424733811
Gene: OR13G1 HGNC NCBI

Linked Data

COSMIC: COSM907067
MyVariant Identifiers: chr1:g.247835957G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672655G>A , CM000663.2:g.247672655G>A GRCh38
NC_000001.10:g.247835957G>A , CM000663.1:g.247835957G>A GRCh37
NC_000001.9:g.245902580G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.387C>T ENSP00000352717.2:p.Tyr129=
ENST00000642119.1:c.387C>T MANE Select ENSP00000493110.1:p.Tyr129=
ENST00000359688.3:c.387C>T ENSP00000352717.2:p.Tyr129=
NM_001005487.1:c.387C>T NP_001005487.1:p.Tyr129=
NM_001005487.2:c.387C>T MANE Select NP_001005487.1:p.Tyr129=
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