Canonical Allele Identifier: CA2807429778
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436561A>C , CM000678.2:g.67436561A>C GRCh38
NC_000016.9:g.67470464A>C , CM000678.1:g.67470464A>C GRCh37
NC_000016.8:g.66027965A>C NCBI36
NG_011482.1:g.49626T>G
NG_016549.1:g.10429A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-27A>C MANE Select ENSP00000316786.5:n.803-27A>C
ENST00000326152.5:c.803-27A>C ENSP00000316786.5:n.803-27A>C
NM_000196.3:c.803-27A>C NP_000187.3:n.803-27A>C
NM_000196.4:c.803-27A>C MANE Select NP_000187.3:n.803-27A>C