Canonical Allele Identifier: CA2484330265
Gene: HSD11B1 HGNC NCBI
HSD11B1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209702170T>G , CM000663.2:g.209702170T>G GRCh38
NC_000001.10:g.209875515T>G , CM000663.1:g.209875515T>G GRCh37
NC_000001.9:g.207942138T>G NCBI36
NG_012081.1:g.20966T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261465.5:c.-48-2725T>G (HSD11B1) ENSP00000261465.2:n.-48-2725T>G
ENST00000367028.6:c.-48-2725T>G (HSD11B1) ENSP00000355995.1:n.-48-2725T>G
ENST00000615289.4:c.-26-2747T>G (HSD11B1) ENSP00000478430.1:n.-26-2747T>G
NM_001206741.1:c.-48-2725T>G (HSD11B1) NP_001193670.1:n.-48-2725T>G
NM_181755.2:c.-26-2747T>G (HSD11B1) NP_861420.1:n.-26-2747T>G
XR_922542.1:n.3234+21860A>C (HSD11B1-AS1)
XR_922543.1:n.3225+21860A>C (HSD11B1-AS1)
XR_922547.1:n.3091-39109A>C (HSD11B1-AS1)
XR_922549.1:n.125-39109A>C (HSD11B1-AS1)
NR_134509.1:n.96+21860A>C (HSD11B1-AS1)
NR_134510.1:n.67-39109A>C (HSD11B1-AS1)
NM_001206741.2:c.-48-2725T>G (HSD11B1) NP_001193670.1:n.-48-2725T>G
NM_181755.3:c.-26-2747T>G (HSD11B1) NP_861420.1:n.-26-2747T>G
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