Canonical Allele Identifier: CA2633779366

Gene: HSD11B2

Linked Data

• gnomAD v4: 16-67436172-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436172G>T , CM000678.2:g.67436172G>T	GRCh38
NC_000016.9:g.67470075G>T , CM000678.1:g.67470075G>T	GRCh37
NC_000016.8:g.66027576G>T	NCBI36
NG_011482.1:g.50015C>A
NG_016549.1:g.10040G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326152.6:c.664+30G>T MANE Select	ENSP00000316786.5:n.664+30G>T
ENST00000326152.5:c.664+30G>T	ENSP00000316786.5:n.664+30G>T
ENST00000567684.2:n.527+30G>T
NM_000196.3:c.664+30G>T	NP_000187.3:n.664+30G>T
NM_000196.4:c.664+30G>T MANE Select	NP_000187.3:n.664+30G>T