Canonical Allele Identifier: CA2484330169
Gene: HSD11B1 HGNC NCBI
HSD11B1-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209701909A>C , CM000663.2:g.209701909A>C GRCh38
NC_000001.10:g.209875254A>C , CM000663.1:g.209875254A>C GRCh37
NC_000001.9:g.207941877A>C NCBI36
NG_012081.1:g.20705A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261465.5:c.-48-2986A>C (HSD11B1) ENSP00000261465.2:n.-48-2986A>C
ENST00000367028.6:c.-48-2986A>C (HSD11B1) ENSP00000355995.1:n.-48-2986A>C
ENST00000615289.4:c.-26-3008A>C (HSD11B1) ENSP00000478430.1:n.-26-3008A>C
NM_001206741.1:c.-48-2986A>C (HSD11B1) NP_001193670.1:n.-48-2986A>C
NM_181755.2:c.-26-3008A>C (HSD11B1) NP_861420.1:n.-26-3008A>C
XR_922542.1:n.3234+22121T>G (HSD11B1-AS1)
XR_922543.1:n.3225+22121T>G (HSD11B1-AS1)
XR_922547.1:n.3091-38848T>G (HSD11B1-AS1)
XR_922549.1:n.125-38848T>G (HSD11B1-AS1)
NR_134509.1:n.96+22121T>G (HSD11B1-AS1)
NR_134510.1:n.67-38848T>G (HSD11B1-AS1)
NM_001206741.2:c.-48-2986A>C (HSD11B1) NP_001193670.1:n.-48-2986A>C
NM_181755.3:c.-26-3008A>C (HSD11B1) NP_861420.1:n.-26-3008A>C
Search 100 bp 5'
Search 100 bp 3'