Canonical Allele Identifier: CA2229310912
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436953G= , CM000678.2:g.67436953G= GRCh38
NC_000016.9:g.67470856G= , CM000678.1:g.67470856G= GRCh37
NC_000016.8:g.66028357G= NCBI36
NG_011482.1:g.49234C=
NG_016549.1:g.10821G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.1168G= MANE Select ENSP00000316786.5:p.Ala390=
ENST00000326152.5:c.1168G= ENSP00000316786.5:p.Ala390=
NM_000196.3:c.1168G= NP_000187.3:p.Ala390=
NM_000196.4:c.1168G= MANE Select NP_000187.3:p.Ala390=