Canonical Allele Identifier: CA36757259
Gene: HSD11B1 HGNC NCBI
HSD11B1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs957380688
MyVariant Identifiers: chr1:g.209885242A>G (hg19) chr1:g.209711897A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209711897A>G , CM000663.2:g.209711897A>G GRCh38
NC_000001.10:g.209885242A>G , CM000663.1:g.209885242A>G GRCh37
NC_000001.9:g.207951865A>G NCBI36
NG_012081.1:g.30693A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367027.5:c.517+4769A>G (HSD11B1) MANE Select ENSP00000355994.3:n.517+4769A>G
ENST00000261465.5:c.517+4769A>G (HSD11B1) ENSP00000261465.2:n.517+4769A>G
ENST00000367027.4:c.517+4769A>G (HSD11B1) ENSP00000355994.3:n.517+4769A>G
ENST00000367028.6:c.517+4769A>G (HSD11B1) ENSP00000355995.1:n.517+4769A>G
ENST00000615289.4:c.517+4769A>G (HSD11B1) ENSP00000478430.1:n.517+4769A>G
NM_001206741.1:c.517+4769A>G (HSD11B1) NP_001193670.1:n.517+4769A>G
NM_005525.3:c.517+4769A>G (HSD11B1) NP_005516.1:n.517+4769A>G
NM_181755.2:c.517+4769A>G (HSD11B1) NP_861420.1:n.517+4769A>G
XR_922542.1:n.3234+12133T>C (HSD11B1-AS1)
XR_922543.1:n.3225+12133T>C (HSD11B1-AS1)
XR_922547.1:n.3090+30600T>C (HSD11B1-AS1)
XR_922549.1:n.124+45579T>C (HSD11B1-AS1)
NR_134509.1:n.96+12133T>C (HSD11B1-AS1)
NR_134510.1:n.66+30600T>C (HSD11B1-AS1)
NM_005525.4:c.517+4769A>G (HSD11B1) MANE Select NP_005516.1:n.517+4769A>G
NM_001206741.2:c.517+4769A>G (HSD11B1) NP_001193670.1:n.517+4769A>G
NM_181755.3:c.517+4769A>G (HSD11B1) NP_861420.1:n.517+4769A>G
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