Canonical Allele Identifier: CA2484324426

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209687265C= , CM000663.2:g.209687265C=	GRCh38
NC_000001.10:g.209860610C= , CM000663.1:g.209860610C=	GRCh37
NC_000001.9:g.207927233C=	NCBI36
NG_012081.1:g.6061C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261465.5:c.-49+980C= (HSD11B1)	ENSP00000261465.2:n.-49+980C=
ENST00000367028.6:c.-49+980C= (HSD11B1)	ENSP00000355995.1:n.-49+980C=
ENST00000615289.4:c.-27+980C= (HSD11B1)	ENSP00000478430.1:n.-27+980C=
NM_001206741.1:c.-49+980C= (HSD11B1)	NP_001193670.1:n.-49+980C=
NM_181755.2:c.-27+980C= (HSD11B1)	NP_861420.1:n.-27+980C=
XR_922538.1:n.1747G=
XR_922539.1:n.1747G=
XR_922540.1:n.113G=
XR_922542.1:n.3235-10732G= (HSD11B1-AS1)
XR_922543.1:n.3226-24204G= (HSD11B1-AS1)
XR_922547.1:n.3091-24204G= (HSD11B1-AS1)
XR_922549.1:n.125-24204G= (HSD11B1-AS1)
NR_134509.1:n.97-24204G= (HSD11B1-AS1)
NR_134510.1:n.67-24204G= (HSD11B1-AS1)
NM_001206741.2:c.-49+980C= (HSD11B1)	NP_001193670.1:n.-49+980C=
NM_181755.3:c.-27+980C= (HSD11B1)	NP_861420.1:n.-27+980C=