Canonical Allele Identifier: CA396279570
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436103A>G , CM000678.2:g.67436103A>G GRCh38
NC_000016.9:g.67470006A>G , CM000678.1:g.67470006A>G GRCh37
NC_000016.8:g.66027507A>G NCBI36
NG_011482.1:g.50084T>C
NG_016549.1:g.9971A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.625A>G MANE Select ENSP00000316786.5:p.Ser209Gly
ENST00000326152.5:c.625A>G ENSP00000316786.5:p.Ser209Gly
ENST00000566606.1:c.603A>G ENSP00000473429.1:n.603A>G
ENST00000567684.2:n.488A>G
NM_000196.3:c.625A>G NP_000187.3:p.Ser209Gly
NM_000196.4:c.625A>G MANE Select NP_000187.3:p.Ser209Gly