Canonical Allele Identifier: CA2229309693
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436088C= , CM000678.2:g.67436088C= GRCh38
NC_000016.9:g.67469991C= , CM000678.1:g.67469991C= GRCh37
NC_000016.8:g.66027492C= NCBI36
NG_011482.1:g.50099G=
NG_016549.1:g.9956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.610C= MANE Select ENSP00000316786.5:p.Leu204=
ENST00000326152.5:c.610C= ENSP00000316786.5:p.Leu204=
ENST00000566606.1:c.588C= ENSP00000473429.1:n.588C=
ENST00000567684.2:n.473C=
NM_000196.3:c.610C= NP_000187.3:p.Leu204=
NM_000196.4:c.610C= MANE Select NP_000187.3:p.Leu204=