Canonical Allele Identifier: CA345563966
Gene: OR13G1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.247835962G>T (hg19) chr1:g.247672660G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672660G>T , CM000663.2:g.247672660G>T GRCh38
NC_000001.10:g.247835962G>T , CM000663.1:g.247835962G>T GRCh37
NC_000001.9:g.245902585G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.382C>A ENSP00000352717.2:p.His128Asn
ENST00000642119.1:c.382C>A MANE Select ENSP00000493110.1:p.His128Asn
ENST00000359688.3:c.382C>A ENSP00000352717.2:p.His128Asn
NM_001005487.1:c.382C>A NP_001005487.1:p.His128Asn
NM_001005487.2:c.382C>A MANE Select NP_001005487.1:p.His128Asn
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