Canonical Allele Identifier: CA496082652

Gene: HSD11B2

Linked Data

• MyVariant Identifiers: chr16:g.67469939T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436036T>A , CM000678.2:g.67436036T>A	GRCh38
NC_000016.9:g.67469939T>A , CM000678.1:g.67469939T>A	GRCh37
NC_000016.8:g.66027440T>A	NCBI36
NG_011482.1:g.50151A>T
NG_016549.1:g.9904T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.558T>A MANE Select	ENSP00000316786.5:p.Arg186=
ENST00000326152.5:c.558T>A	ENSP00000316786.5:p.Arg186=
ENST00000566606.1:c.536T>A	ENSP00000473429.1:n.536T>A
ENST00000567684.2:n.421T>A
NM_000196.3:c.558T>A	NP_000187.3:p.Arg186=
NM_000196.4:c.558T>A MANE Select	NP_000187.3:p.Arg186=