Canonical Allele Identifier: CA2229311082
Gene: HSD11B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67437093C= , CM000678.2:g.67437093C= GRCh38
NC_000016.9:g.67470996C= , CM000678.1:g.67470996C= GRCh37
NC_000016.8:g.66028497C= NCBI36
NG_011482.1:g.49094G=
NG_016549.1:g.10961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.*90C= MANE Select ENSP00000316786.5:n.*90C=
ENST00000326152.5:c.*90C= ENSP00000316786.5:n.*90C=
NM_000196.3:c.*90C= NP_000187.3:n.*90C=
NM_000196.4:c.*90C= MANE Select NP_000187.3:n.*90C=
Search 100 bp 5'
Search 100 bp 3'