Canonical Allele Identifier: CA344581169

Gene: HSD11B1 HSD11B1-AS1

Linked Data

• MyVariant Identifiers: chr1:g.209880124C>G (hg19) ; chr1:g.209706779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209706779C>G , CM000663.2:g.209706779C>G	GRCh38
NC_000001.10:g.209880124C>G , CM000663.1:g.209880124C>G	GRCh37
NC_000001.9:g.207946747C>G	NCBI36
NG_012081.1:g.25575C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367027.5:c.290C>G (HSD11B1) MANE Select	ENSP00000355994.3:p.Thr97Ser
ENST00000261465.5:c.290C>G (HSD11B1)	ENSP00000261465.2:p.Thr97Ser
ENST00000367027.4:c.290C>G (HSD11B1)	ENSP00000355994.3:p.Thr97Ser
ENST00000367028.6:c.290C>G (HSD11B1)	ENSP00000355995.1:p.Thr97Ser
ENST00000615289.4:c.290C>G (HSD11B1)	ENSP00000478430.1:p.Thr97Ser
NM_001206741.1:c.290C>G (HSD11B1)	NP_001193670.1:p.Thr97Ser
NM_005525.3:c.290C>G (HSD11B1)	NP_005516.1:p.Thr97Ser
NM_181755.2:c.290C>G (HSD11B1)	NP_861420.1:p.Thr97Ser
XR_922542.1:n.3234+17251G>C (HSD11B1-AS1)
XR_922543.1:n.3225+17251G>C (HSD11B1-AS1)
XR_922547.1:n.3090+35718G>C (HSD11B1-AS1)
XR_922549.1:n.125-43718G>C (HSD11B1-AS1)
NR_134509.1:n.96+17251G>C (HSD11B1-AS1)
NR_134510.1:n.66+35718G>C (HSD11B1-AS1)
NM_005525.4:c.290C>G (HSD11B1) MANE Select	NP_005516.1:p.Thr97Ser
NM_001206741.2:c.290C>G (HSD11B1)	NP_001193670.1:p.Thr97Ser
NM_181755.3:c.290C>G (HSD11B1)	NP_861420.1:p.Thr97Ser