Canonical Allele Identifier: CA396279455
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436082G>A , CM000678.2:g.67436082G>A GRCh38
NC_000016.9:g.67469985G>A , CM000678.1:g.67469985G>A GRCh37
NC_000016.8:g.66027486G>A NCBI36
NG_011482.1:g.50105C>T
NG_016549.1:g.9950G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.604G>A MANE Select ENSP00000316786.5:p.Gly202Ser
ENST00000326152.5:c.604G>A ENSP00000316786.5:p.Gly202Ser
ENST00000566606.1:c.582G>A ENSP00000473429.1:n.582G>A
ENST00000567684.2:n.467G>A
NM_000196.3:c.604G>A NP_000187.3:p.Gly202Ser
NM_000196.4:c.604G>A MANE Select NP_000187.3:p.Gly202Ser