Canonical Allele Identifier: CA2229309132
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435560G= , CM000678.2:g.67435560G= GRCh38
NC_000016.9:g.67469463G= , CM000678.1:g.67469463G= GRCh37
NC_000016.8:g.66026964G= NCBI36
NG_016549.1:g.9428G=

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.266-68G= MANE Select ENSP00000316786.5:n.266-68G=
ENST00000326152.5:c.266-68G= ENSP00000316786.5:n.266-68G=
ENST00000566606.1:c.176G= ENSP00000473429.1:p.Ter59=
ENST00000567684.2:n.129-68G=
NM_000196.3:c.266-68G= NP_000187.3:n.266-68G=
NM_000196.4:c.266-68G= MANE Select NP_000187.3:n.266-68G=
Search 100 bp 5'
Search 100 bp 3'