Canonical Allele Identifier: CA2229309616
Gene: HSD11B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436034C= , CM000678.2:g.67436034C= GRCh38
NC_000016.9:g.67469937C= , CM000678.1:g.67469937C= GRCh37
NC_000016.8:g.66027438C= NCBI36
NG_011482.1:g.50153G=
NG_016549.1:g.9902C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.556C= MANE Select ENSP00000316786.5:p.Arg186=
ENST00000326152.5:c.556C= ENSP00000316786.5:p.Arg186=
ENST00000566606.1:c.534C= ENSP00000473429.1:n.534C=
ENST00000567684.2:n.419C=
NM_000196.3:c.556C= NP_000187.3:p.Arg186=
NM_000196.4:c.556C= MANE Select NP_000187.3:p.Arg186=
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