Canonical Allele Identifier: CA2229311064
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437085A= , CM000678.2:g.67437085A= GRCh38
NC_000016.9:g.67470988A= , CM000678.1:g.67470988A= GRCh37
NC_000016.8:g.66028489A= NCBI36
NG_011482.1:g.49102T=
NG_016549.1:g.10953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*82A= MANE Select ENSP00000316786.5:n.*82A=
ENST00000326152.5:c.*82A= ENSP00000316786.5:n.*82A=
NM_000196.3:c.*82A= NP_000187.3:n.*82A=
NM_000196.4:c.*82A= MANE Select NP_000187.3:n.*82A=
Search 100 bp 5'
Search 100 bp 3'