Canonical Allele Identifier: CA496082459

Gene: HSD11B2

Linked Data

• MyVariant Identifiers: chr16:g.67469885A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435982A>C , CM000678.2:g.67435982A>C	GRCh38
NC_000016.9:g.67469885A>C , CM000678.1:g.67469885A>C	GRCh37
NC_000016.8:g.66027386A>C	NCBI36
NG_016549.1:g.9850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.504A>C MANE Select	ENSP00000316786.5:p.Ala168=
ENST00000326152.5:c.504A>C	ENSP00000316786.5:p.Ala168=
ENST00000566606.1:c.482A>C	ENSP00000473429.1:n.482A>C
ENST00000567684.2:n.367A>C
NM_000196.3:c.504A>C	NP_000187.3:p.Ala168=
NM_000196.4:c.504A>C MANE Select	NP_000187.3:p.Ala168=