Canonical Allele Identifier: CA396282938

Gene: HSD11B2

Linked Data

• MyVariant Identifiers: chr16:g.67470694C>G (hg19) ; chr16:g.67436791C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436791C>G , CM000678.2:g.67436791C>G	GRCh38
NC_000016.9:g.67470694C>G , CM000678.1:g.67470694C>G	GRCh37
NC_000016.8:g.66028195C>G	NCBI36
NG_011482.1:g.49396G>C
NG_016549.1:g.10659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.1006C>G MANE Select	ENSP00000316786.5:p.Arg336Gly
ENST00000326152.5:c.1006C>G	ENSP00000316786.5:p.Arg336Gly
NM_000196.3:c.1006C>G	NP_000187.3:p.Arg336Gly
NM_000196.4:c.1006C>G MANE Select	NP_000187.3:p.Arg336Gly