Canonical Allele Identifier: CA1496904
Gene: OR13G1 HGNC NCBI

Linked Data

dbSNP Id: rs76372161
ExAC: 1:247835961 T / C
gnomAD v2: 1-247835961-T-C
gnomAD v3: 1-247672659-T-C
gnomAD v4: 1-247672659-T-C
MyVariant Identifiers: chr1:g.247835961T>C (hg19) chr1:g.247672659T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247672659T>C , CM000663.2:g.247672659T>C GRCh38
NC_000001.10:g.247835961T>C , CM000663.1:g.247835961T>C GRCh37
NC_000001.9:g.245902584T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000359688.4:c.383A>G ENSP00000352717.2:p.His128Arg
ENST00000642119.1:c.383A>G MANE Select ENSP00000493110.1:p.His128Arg
ENST00000359688.3:c.383A>G ENSP00000352717.2:p.His128Arg
NM_001005487.1:c.383A>G NP_001005487.1:p.His128Arg
NM_001005487.2:c.383A>G MANE Select NP_001005487.1:p.His128Arg
Search 100 bp 5'
Search 100 bp 3'