Canonical Allele Identifier: CA1139835531

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209701909A= , CM000663.2:g.209701909A=	GRCh38
NC_000001.10:g.209875254A= , CM000663.1:g.209875254A=	GRCh37
NC_000001.9:g.207941877A=	NCBI36
NG_012081.1:g.20705A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261465.5:c.-48-2986A= (HSD11B1)	ENSP00000261465.2:n.-48-2986A=
ENST00000367028.6:c.-48-2986A= (HSD11B1)	ENSP00000355995.1:n.-48-2986A=
ENST00000615289.4:c.-26-3008A= (HSD11B1)	ENSP00000478430.1:n.-26-3008A=
NM_001206741.1:c.-48-2986A= (HSD11B1)	NP_001193670.1:n.-48-2986A=
NM_181755.2:c.-26-3008A= (HSD11B1)	NP_861420.1:n.-26-3008A=
XR_922542.1:n.3234+22121T= (HSD11B1-AS1)
XR_922543.1:n.3225+22121T= (HSD11B1-AS1)
XR_922547.1:n.3091-38848T= (HSD11B1-AS1)
XR_922549.1:n.125-38848T= (HSD11B1-AS1)
NR_134509.1:n.96+22121T= (HSD11B1-AS1)
NR_134510.1:n.67-38848T= (HSD11B1-AS1)
NM_001206741.2:c.-48-2986A= (HSD11B1)	NP_001193670.1:n.-48-2986A=
NM_181755.3:c.-26-3008A= (HSD11B1)	NP_861420.1:n.-26-3008A=