Canonical Allele Identifier: CA345563929
Gene: OR13G1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.247835955C>G (hg19) chr1:g.247672653C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672653C>G , CM000663.2:g.247672653C>G GRCh38
NC_000001.10:g.247835955C>G , CM000663.1:g.247835955C>G GRCh37
NC_000001.9:g.245902578C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.389G>C ENSP00000352717.2:p.Ser130Thr
ENST00000642119.1:c.389G>C MANE Select ENSP00000493110.1:p.Ser130Thr
ENST00000359688.3:c.389G>C ENSP00000352717.2:p.Ser130Thr
NM_001005487.1:c.389G>C NP_001005487.1:p.Ser130Thr
NM_001005487.2:c.389G>C MANE Select NP_001005487.1:p.Ser130Thr
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