Canonical Allele Identifier: CA2229310553
Gene: HSD11B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436736C= , CM000678.2:g.67436736C= GRCh38
NC_000016.9:g.67470639C= , CM000678.1:g.67470639C= GRCh37
NC_000016.8:g.66028140C= NCBI36
NG_011482.1:g.49451G=
NG_016549.1:g.10604C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.951C= MANE Select ENSP00000316786.5:p.Asp317=
ENST00000326152.5:c.951C= ENSP00000316786.5:p.Asp317=
NM_000196.3:c.951C= NP_000187.3:p.Asp317=
NM_000196.4:c.951C= MANE Select NP_000187.3:p.Asp317=
Search 100 bp 5'
Search 100 bp 3'