Canonical Allele Identifier: CA396279172
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs774383256

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436040T>G , CM000678.2:g.67436040T>G GRCh38
NC_000016.9:g.67469943T>G , CM000678.1:g.67469943T>G GRCh37
NC_000016.8:g.66027444T>G NCBI36
NG_011482.1:g.50147A>C
NG_016549.1:g.9908T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.562T>G MANE Select ENSP00000316786.5:p.Cys188Gly
ENST00000326152.5:c.562T>G ENSP00000316786.5:p.Cys188Gly
ENST00000566606.1:c.540T>G ENSP00000473429.1:n.540T>G
ENST00000567684.2:n.425T>G
NM_000196.3:c.562T>G NP_000187.3:p.Cys188Gly
NM_000196.4:c.562T>G MANE Select NP_000187.3:p.Cys188Gly