Canonical Allele Identifier: CA2576029122
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67435531-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435531A>T , CM000678.2:g.67435531A>T GRCh38
NC_000016.9:g.67469434A>T , CM000678.1:g.67469434A>T GRCh37
NC_000016.8:g.66026935A>T NCBI36
NG_016549.1:g.9399A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.266-97A>T MANE Select ENSP00000316786.5:n.266-97A>T
ENST00000326152.5:c.266-97A>T ENSP00000316786.5:n.266-97A>T
ENST00000566606.1:c.149-2A>T ENSP00000473429.1:n.149-2A>T
ENST00000567684.2:n.129-97A>T
NM_000196.3:c.266-97A>T NP_000187.3:n.266-97A>T
NM_000196.4:c.266-97A>T MANE Select NP_000187.3:n.266-97A>T
Search 100 bp 5'
Search 100 bp 3'