Canonical Allele Identifier: CA1139846542

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209721316G= , CM000663.2:g.209721316G=	GRCh38
NC_000001.10:g.209894661G= , CM000663.1:g.209894661G=	GRCh37
NC_000001.9:g.207961284G=	NCBI36
NG_012081.1:g.40112G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005525.4:c.518-11120G= (HSD11B1) MANE Select	NP_005516.1:n.518-11120G=
ENST00000367027.5:c.518-11120G= (HSD11B1) MANE Select	ENSP00000355994.3:n.518-11120G=
NM_001206741.1:c.518-11120G= (HSD11B1)	NP_001193670.1:n.518-11120G=
NM_001206741.2:c.518-11120G= (HSD11B1)	NP_001193670.1:n.518-11120G=
NM_005525.3:c.518-11120G= (HSD11B1)	NP_005516.1:n.518-11120G=
NM_181755.2:c.518-11120G= (HSD11B1)	NP_861420.1:n.518-11120G=
NM_181755.3:c.518-11120G= (HSD11B1)	NP_861420.1:n.518-11120G=
NR_134509.1:n.96+2714C= (HSD11B1-AS1)
NR_134510.1:n.66+21181C= (HSD11B1-AS1)
ENST00000261465.5:c.518-11120G= (HSD11B1)	ENSP00000261465.2:n.518-11120G=
ENST00000367027.4:c.518-11120G= (HSD11B1)	ENSP00000355994.3:n.518-11120G=
ENST00000367028.6:c.518-11120G= (HSD11B1)	ENSP00000355995.1:n.518-11120G=
ENST00000615289.4:c.518-11120G= (HSD11B1)	ENSP00000478430.1:n.518-11120G=
XR_922542.1:n.3234+2714C= (HSD11B1-AS1)
XR_922543.1:n.3225+2714C= (HSD11B1-AS1)
XR_922547.1:n.3090+21181C= (HSD11B1-AS1)
XR_922549.1:n.124+36160C= (HSD11B1-AS1)