Canonical Allele Identifier: CA2229309911
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436202G= , CM000678.2:g.67436202G= GRCh38
NC_000016.9:g.67470105G= , CM000678.1:g.67470105G= GRCh37
NC_000016.8:g.66027606G= NCBI36
NG_011482.1:g.49985C=
NG_016549.1:g.10070G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.665-47G= MANE Select ENSP00000316786.5:n.665-47G=
ENST00000326152.5:c.665-47G= ENSP00000316786.5:n.665-47G=
ENST00000567684.2:n.528-47G=
NM_000196.3:c.665-47G= NP_000187.3:n.665-47G=
NM_000196.4:c.665-47G= MANE Select NP_000187.3:n.665-47G=
Search 100 bp 5'
Search 100 bp 3'