Canonical Allele Identifier: CA36753489

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

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

Transcript Alleles

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