Canonical Allele Identifier: CA8110756
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs777046730

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436584C>G , CM000678.2:g.67436584C>G GRCh38
NC_000016.9:g.67470487C>G , CM000678.1:g.67470487C>G GRCh37
NC_000016.8:g.66027988C>G NCBI36
NG_011482.1:g.49603G>C
NG_016549.1:g.10452C>G

Transcript Alleles

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