Canonical Allele Identifier: CA496082498

Gene: HSD11B2

Linked Data

• MyVariant Identifiers: chr16:g.67469906T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436003T>G , CM000678.2:g.67436003T>G	GRCh38
NC_000016.9:g.67469906T>G , CM000678.1:g.67469906T>G	GRCh37
NC_000016.8:g.66027407T>G	NCBI36
NG_016549.1:g.9871T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.525T>G MANE Select	ENSP00000316786.5:p.Ala175=
ENST00000326152.5:c.525T>G	ENSP00000316786.5:p.Ala175=
ENST00000566606.1:c.503T>G	ENSP00000473429.1:n.503T>G
ENST00000567684.2:n.388T>G
NM_000196.3:c.525T>G	NP_000187.3:p.Ala175=
NM_000196.4:c.525T>G MANE Select	NP_000187.3:p.Ala175=