Canonical Allele Identifier: CA2633779292

Gene: HSD11B2

Linked Data

• gnomAD v4: 16-67436147-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67436147G>C , CM000678.2:g.67436147G>C	GRCh38
NC_000016.9:g.67470050G>C , CM000678.1:g.67470050G>C	GRCh37
NC_000016.8:g.66027551G>C	NCBI36
NG_011482.1:g.50040C>G
NG_016549.1:g.10015G>C

Transcript Alleles

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