Canonical Allele Identifier: CA2651430362
Gene: OR2B11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247457761T>C , CM000663.2:g.247457761T>C GRCh38
NC_000001.10:g.247621063T>C , CM000663.1:g.247621063T>C GRCh37
NC_000001.9:g.245687686T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641149.2:c.-3205A>G MANE Select ENSP00000492892.1:n.-3205A>G
ENST00000641149.1:c.-3205A>G ENSP00000492892.1:n.-3205A>G
ENST00000641527.1:c.-1336A>G ENSP00000493421.1:n.-1336A>G
ENST00000641613.1:n.248A>G
NM_001004492.2:c.-3205A>G MANE Select NP_001004492.1:n.-3205A>G
NR_169840.1:n.248A>G