Canonical Allele Identifier: CA2229311075
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437089T= , CM000678.2:g.67437089T= GRCh38
NC_000016.9:g.67470992T= , CM000678.1:g.67470992T= GRCh37
NC_000016.8:g.66028493T= NCBI36
NG_011482.1:g.49098A=
NG_016549.1:g.10957T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*86T= MANE Select ENSP00000316786.5:n.*86T=
ENST00000326152.5:c.*86T= ENSP00000316786.5:n.*86T=
NM_000196.3:c.*86T= NP_000187.3:n.*86T=
NM_000196.4:c.*86T= MANE Select NP_000187.3:n.*86T=
Search 100 bp 5'
Search 100 bp 3'