Canonical Allele Identifier: CA2576029168
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436251del , CM000678.2:g.67436251del GRCh38
NC_000016.9:g.67470154del , CM000678.1:g.67470154del GRCh37
NC_000016.8:g.66027655del NCBI36
NG_011482.1:g.49939del
NG_016549.1:g.10119del

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.667del
ENST00000326152.5:c.667del
ENST00000567684.2:n.530del
NM_000196.3:c.667del
NM_000196.4:c.667del