Canonical Allele Identifier: CA2633778697
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67435536-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435536C>A , CM000678.2:g.67435536C>A GRCh38
NC_000016.9:g.67469439C>A , CM000678.1:g.67469439C>A GRCh37
NC_000016.8:g.66026940C>A NCBI36
NG_016549.1:g.9404C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.266-92C>A MANE Select ENSP00000316786.5:n.266-92C>A
ENST00000326152.5:c.266-92C>A ENSP00000316786.5:n.266-92C>A
ENST00000566606.1:c.152C>A ENSP00000473429.1:p.Ala51Asp
ENST00000567684.2:n.129-92C>A
NM_000196.3:c.266-92C>A NP_000187.3:n.266-92C>A
NM_000196.4:c.266-92C>A MANE Select NP_000187.3:n.266-92C>A
Search 100 bp 5'
Search 100 bp 3'