Canonical Allele Identifier: CA2651430359
Gene: OR2B11 HGNC NCBI

Linked Data

gnomAD v4: 1-247457756-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247457756C>T , CM000663.2:g.247457756C>T GRCh38
NC_000001.10:g.247621058C>T , CM000663.1:g.247621058C>T GRCh37
NC_000001.9:g.245687681C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641149.2:c.-3200G>A MANE Select ENSP00000492892.1:n.-3200G>A
ENST00000641149.1:c.-3200G>A ENSP00000492892.1:n.-3200G>A
ENST00000641527.1:c.-1331G>A ENSP00000493421.1:n.-1331G>A
ENST00000641613.1:n.253G>A
NM_001004492.2:c.-3200G>A MANE Select NP_001004492.1:n.-3200G>A
NR_169840.1:n.253G>A
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