Canonical Allele Identifier: CA723046844

Gene: HSD11B2

Linked Data

• dbSNP Id: rs1194473038
• MyVariant Identifiers: chr16:g.67469494C>T (hg19) ; chr16:g.67435591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67435591C>T , CM000678.2:g.67435591C>T	GRCh38
NC_000016.9:g.67469494C>T , CM000678.1:g.67469494C>T	GRCh37
NC_000016.8:g.66026995C>T	NCBI36
NG_016549.1:g.9459C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.266-37C>T MANE Select	ENSP00000316786.5:n.266-37C>T
ENST00000326152.5:c.266-37C>T	ENSP00000316786.5:n.266-37C>T
ENST00000566606.1:c.207C>T	ENSP00000473429.1:n.207C>T
ENST00000567684.2:n.129-37C>T
NM_000196.3:c.266-37C>T	NP_000187.3:n.266-37C>T
NM_000196.4:c.266-37C>T MANE Select	NP_000187.3:n.266-37C>T