Canonical Allele Identifier: CA8110770
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs758672428

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436692T>C , CM000678.2:g.67436692T>C GRCh38
NC_000016.9:g.67470595T>C , CM000678.1:g.67470595T>C GRCh37
NC_000016.8:g.66028096T>C NCBI36
NG_011482.1:g.49495A>G
NG_016549.1:g.10560T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.907T>C MANE Select ENSP00000316786.5:p.Leu303=
ENST00000326152.5:c.907T>C ENSP00000316786.5:p.Leu303=
NM_000196.3:c.907T>C NP_000187.3:p.Leu303=
NM_000196.4:c.907T>C MANE Select NP_000187.3:p.Leu303=