Canonical Allele Identifier: CA2229310333
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436568C= , CM000678.2:g.67436568C= GRCh38
NC_000016.9:g.67470471C= , CM000678.1:g.67470471C= GRCh37
NC_000016.8:g.66027972C= NCBI36
NG_011482.1:g.49619G=
NG_016549.1:g.10436C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-20C= MANE Select ENSP00000316786.5:n.803-20C=
ENST00000326152.5:c.803-20C= ENSP00000316786.5:n.803-20C=
NM_000196.3:c.803-20C= NP_000187.3:n.803-20C=
NM_000196.4:c.803-20C= MANE Select NP_000187.3:n.803-20C=
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