Canonical Allele Identifier: CA345563926
Gene: OR13G1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.247835954A>C (hg19) chr1:g.247672652A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672652A>C , CM000663.2:g.247672652A>C GRCh38
NC_000001.10:g.247835954A>C , CM000663.1:g.247835954A>C GRCh37
NC_000001.9:g.245902577A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.390T>G ENSP00000352717.2:p.Ser130Arg
ENST00000642119.1:c.390T>G MANE Select ENSP00000493110.1:p.Ser130Arg
ENST00000359688.3:c.390T>G ENSP00000352717.2:p.Ser130Arg
NM_001005487.1:c.390T>G NP_001005487.1:p.Ser130Arg
NM_001005487.2:c.390T>G MANE Select NP_001005487.1:p.Ser130Arg
Search 100 bp 5'
Search 100 bp 3'