Canonical Allele Identifier: CA496082649

Gene: HSD11B2

Linked Data

• MyVariant Identifiers: chr16:g.67469933T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436030T>G , CM000678.2:g.67436030T>G	GRCh38
NC_000016.9:g.67469933T>G , CM000678.1:g.67469933T>G	GRCh37
NC_000016.8:g.66027434T>G	NCBI36
NG_011482.1:g.50157A>C
NG_016549.1:g.9898T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.552T>G MANE Select	ENSP00000316786.5:p.Thr184=
ENST00000326152.5:c.552T>G	ENSP00000316786.5:p.Thr184=
ENST00000566606.1:c.530T>G	ENSP00000473429.1:n.530T>G
ENST00000567684.2:n.415T>G
NM_000196.3:c.552T>G	NP_000187.3:p.Thr184=
NM_000196.4:c.552T>G MANE Select	NP_000187.3:p.Thr184=