Canonical Allele Identifier: CA730840596

Gene: HSD11B1 HSD11B1-AS1

Linked Data

• dbSNP Id: rs1485937002
• gnomAD v3: 1-209706908-C-T
• gnomAD v4: 1-209706908-C-T
• MyVariant Identifiers: chr1:g.209880253C>T (hg19) ; chr1:g.209706908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209706908C>T , CM000663.2:g.209706908C>T	GRCh38
NC_000001.10:g.209880253C>T , CM000663.1:g.209880253C>T	GRCh37
NC_000001.9:g.207946876C>T	NCBI36
NG_012081.1:g.25704C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367027.5:c.332-35C>T (HSD11B1) MANE Select	ENSP00000355994.3:n.332-35C>T
ENST00000261465.5:c.332-35C>T (HSD11B1)	ENSP00000261465.2:n.332-35C>T
ENST00000367027.4:c.332-35C>T (HSD11B1)	ENSP00000355994.3:n.332-35C>T
ENST00000367028.6:c.332-35C>T (HSD11B1)	ENSP00000355995.1:n.332-35C>T
ENST00000615289.4:c.332-35C>T (HSD11B1)	ENSP00000478430.1:n.332-35C>T
NM_001206741.1:c.332-35C>T (HSD11B1)	NP_001193670.1:n.332-35C>T
NM_005525.3:c.332-35C>T (HSD11B1)	NP_005516.1:n.332-35C>T
NM_181755.2:c.332-35C>T (HSD11B1)	NP_861420.1:n.332-35C>T
XR_922542.1:n.3234+17122G>A (HSD11B1-AS1)
XR_922543.1:n.3225+17122G>A (HSD11B1-AS1)
XR_922547.1:n.3090+35589G>A (HSD11B1-AS1)
XR_922549.1:n.125-43847G>A (HSD11B1-AS1)
NR_134509.1:n.96+17122G>A (HSD11B1-AS1)
NR_134510.1:n.66+35589G>A (HSD11B1-AS1)
NM_005525.4:c.332-35C>T (HSD11B1) MANE Select	NP_005516.1:n.332-35C>T
NM_001206741.2:c.332-35C>T (HSD11B1)	NP_001193670.1:n.332-35C>T
NM_181755.3:c.332-35C>T (HSD11B1)	NP_861420.1:n.332-35C>T