Canonical Allele Identifier: CA36748883

Gene: HSD11B1 HSD11B1-AS1

Linked Data

• dbSNP Id: rs937542009
• MyVariant Identifiers: chr1:g.209860620G>A (hg19) ; chr1:g.209687275G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209687275G>A , CM000663.2:g.209687275G>A	GRCh38
NC_000001.10:g.209860620G>A , CM000663.1:g.209860620G>A	GRCh37
NC_000001.9:g.207927243G>A	NCBI36
NG_012081.1:g.6071G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261465.5:c.-49+990G>A (HSD11B1)	ENSP00000261465.2:n.-49+990G>A
ENST00000367028.6:c.-49+990G>A (HSD11B1)	ENSP00000355995.1:n.-49+990G>A
ENST00000615289.4:c.-27+990G>A (HSD11B1)	ENSP00000478430.1:n.-27+990G>A
NM_001206741.1:c.-49+990G>A (HSD11B1)	NP_001193670.1:n.-49+990G>A
NM_181755.2:c.-27+990G>A (HSD11B1)	NP_861420.1:n.-27+990G>A
XR_922538.1:n.1737C>T
XR_922539.1:n.1737C>T
XR_922540.1:n.103C>T
XR_922542.1:n.3235-10742C>T (HSD11B1-AS1)
XR_922543.1:n.3226-24214C>T (HSD11B1-AS1)
XR_922547.1:n.3091-24214C>T (HSD11B1-AS1)
XR_922549.1:n.125-24214C>T (HSD11B1-AS1)
NR_134509.1:n.97-24214C>T (HSD11B1-AS1)
NR_134510.1:n.67-24214C>T (HSD11B1-AS1)
NM_001206741.2:c.-49+990G>A (HSD11B1)	NP_001193670.1:n.-49+990G>A
NM_181755.3:c.-27+990G>A (HSD11B1)	NP_861420.1:n.-27+990G>A