Canonical Allele Identifier: CA2484328380

Gene: HSD11B1 HSD11B1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209697571A>C , CM000663.2:g.209697571A>C	GRCh38
NC_000001.10:g.209870916A>C , CM000663.1:g.209870916A>C	GRCh37
NC_000001.9:g.207937539A>C	NCBI36
NG_012081.1:g.16367A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261465.5:c.-48-7324A>C (HSD11B1)	ENSP00000261465.2:n.-48-7324A>C
ENST00000367028.6:c.-48-7324A>C (HSD11B1)	ENSP00000355995.1:n.-48-7324A>C
ENST00000615289.4:c.-26-7346A>C (HSD11B1)	ENSP00000478430.1:n.-26-7346A>C
NM_001206741.1:c.-48-7324A>C (HSD11B1)	NP_001193670.1:n.-48-7324A>C
NM_181755.2:c.-26-7346A>C (HSD11B1)	NP_861420.1:n.-26-7346A>C
XR_922542.1:n.3235-21038T>G (HSD11B1-AS1)
XR_922543.1:n.3225+26459T>G (HSD11B1-AS1)
XR_922547.1:n.3091-34510T>G (HSD11B1-AS1)
XR_922549.1:n.125-34510T>G (HSD11B1-AS1)
NR_134509.1:n.96+26459T>G (HSD11B1-AS1)
NR_134510.1:n.67-34510T>G (HSD11B1-AS1)
NM_001206741.2:c.-48-7324A>C (HSD11B1)	NP_001193670.1:n.-48-7324A>C
NM_181755.3:c.-26-7346A>C (HSD11B1)	NP_861420.1:n.-26-7346A>C