Canonical Allele Identifier: CA396279753
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs1373677424

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436127G>A , CM000678.2:g.67436127G>A GRCh38
NC_000016.9:g.67470030G>A , CM000678.1:g.67470030G>A GRCh37
NC_000016.8:g.66027531G>A NCBI36
NG_011482.1:g.50060C>T
NG_016549.1:g.9995G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.649G>A MANE Select ENSP00000316786.5:p.Val217Met
ENST00000326152.5:c.649G>A ENSP00000316786.5:p.Val217Met
ENST00000566606.1:c.627G>A ENSP00000473429.1:n.627G>A
ENST00000567684.2:n.512G>A
NM_000196.3:c.649G>A NP_000187.3:p.Val217Met
NM_000196.4:c.649G>A MANE Select NP_000187.3:p.Val217Met