Canonical Allele Identifier: CA282322933
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs1033239625

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436368C>T , CM000678.2:g.67436368C>T GRCh38
NC_000016.9:g.67470271C>T , CM000678.1:g.67470271C>T GRCh37
NC_000016.8:g.66027772C>T NCBI36
NG_011482.1:g.49819G>A
NG_016549.1:g.10236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.784C>T MANE Select ENSP00000316786.5:p.Pro262Ser
ENST00000326152.5:c.784C>T ENSP00000316786.5:p.Pro262Ser
NM_000196.3:c.784C>T NP_000187.3:p.Pro262Ser
NM_000196.4:c.784C>T MANE Select NP_000187.3:p.Pro262Ser