Canonical Allele Identifier: CA1145626513
Gene: OR2B11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247457760T= , CM000663.2:g.247457760T= GRCh38
NC_000001.10:g.247621062T= , CM000663.1:g.247621062T= GRCh37
NC_000001.9:g.245687685T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641149.2:c.-3204A= MANE Select ENSP00000492892.1:n.-3204A=
ENST00000641149.1:c.-3204A= ENSP00000492892.1:n.-3204A=
ENST00000641527.1:c.-1335A= ENSP00000493421.1:n.-1335A=
ENST00000641613.1:n.249A=
NM_001004492.2:c.-3204A= MANE Select NP_001004492.1:n.-3204A=
NR_169840.1:n.249A=