Canonical Allele Identifier: CA396278839
Gene: HSD11B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435978A>G , CM000678.2:g.67435978A>G GRCh38
NC_000016.9:g.67469881A>G , CM000678.1:g.67469881A>G GRCh37
NC_000016.8:g.66027382A>G NCBI36
NG_016549.1:g.9846A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.500A>G MANE Select ENSP00000316786.5:p.Asn167Ser
ENST00000326152.5:c.500A>G ENSP00000316786.5:p.Asn167Ser
ENST00000566606.1:c.478A>G ENSP00000473429.1:n.478A>G
ENST00000567684.2:n.363A>G
NM_000196.3:c.500A>G NP_000187.3:p.Asn167Ser
NM_000196.4:c.500A>G MANE Select NP_000187.3:p.Asn167Ser