Canonical Allele Identifier: CA1011775839
Gene: HSD11B1 HGNC NCBI
HSD11B1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2076898407
gnomAD v3: 1-209711905-G-T
gnomAD v4: 1-209711905-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209711905G>T , CM000663.2:g.209711905G>T GRCh38
NC_000001.10:g.209885250G>T , CM000663.1:g.209885250G>T GRCh37
NC_000001.9:g.207951873G>T NCBI36
NG_012081.1:g.30701G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367027.5:c.517+4777G>T (HSD11B1) MANE Select ENSP00000355994.3:n.517+4777G>T
ENST00000261465.5:c.517+4777G>T (HSD11B1) ENSP00000261465.2:n.517+4777G>T
ENST00000367027.4:c.517+4777G>T (HSD11B1) ENSP00000355994.3:n.517+4777G>T
ENST00000367028.6:c.517+4777G>T (HSD11B1) ENSP00000355995.1:n.517+4777G>T
ENST00000615289.4:c.517+4777G>T (HSD11B1) ENSP00000478430.1:n.517+4777G>T
NM_001206741.1:c.517+4777G>T (HSD11B1) NP_001193670.1:n.517+4777G>T
NM_005525.3:c.517+4777G>T (HSD11B1) NP_005516.1:n.517+4777G>T
NM_181755.2:c.517+4777G>T (HSD11B1) NP_861420.1:n.517+4777G>T
XR_922542.1:n.3234+12125C>A (HSD11B1-AS1)
XR_922543.1:n.3225+12125C>A (HSD11B1-AS1)
XR_922547.1:n.3090+30592C>A (HSD11B1-AS1)
XR_922549.1:n.124+45571C>A (HSD11B1-AS1)
NR_134509.1:n.96+12125C>A (HSD11B1-AS1)
NR_134510.1:n.66+30592C>A (HSD11B1-AS1)
NM_005525.4:c.517+4777G>T (HSD11B1) MANE Select NP_005516.1:n.517+4777G>T
NM_001206741.2:c.517+4777G>T (HSD11B1) NP_001193670.1:n.517+4777G>T
NM_181755.3:c.517+4777G>T (HSD11B1) NP_861420.1:n.517+4777G>T
Search 100 bp 5'
Search 100 bp 3'