Canonical Allele Identifier: CA2633780136
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67436532-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436532A>G , CM000678.2:g.67436532A>G GRCh38
NC_000016.9:g.67470435A>G , CM000678.1:g.67470435A>G GRCh37
NC_000016.8:g.66027936A>G NCBI36
NG_011482.1:g.49655T>C
NG_016549.1:g.10400A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.803-56A>G MANE Select ENSP00000316786.5:n.803-56A>G
ENST00000326152.5:c.803-56A>G ENSP00000316786.5:n.803-56A>G
NM_000196.3:c.803-56A>G NP_000187.3:n.803-56A>G
NM_000196.4:c.803-56A>G MANE Select NP_000187.3:n.803-56A>G
Search 100 bp 5'
Search 100 bp 3'