Canonical Allele Identifier: CA282321685
Gene: HSD11B2 HGNC NCBI

Linked Data

dbSNP Id: rs758023060
gnomAD v4: 16-67435534-G-A
MyVariant Identifiers: chr16:g.67469437G>A (hg19) chr16:g.67435534G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67435534G>A , CM000678.2:g.67435534G>A GRCh38
NC_000016.9:g.67469437G>A , CM000678.1:g.67469437G>A GRCh37
NC_000016.8:g.66026938G>A NCBI36
NG_016549.1:g.9402G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.266-94G>A MANE Select ENSP00000316786.5:n.266-94G>A
ENST00000326152.5:c.266-94G>A ENSP00000316786.5:n.266-94G>A
ENST00000566606.1:c.150G>A ENSP00000473429.1:p.Gly50=
ENST00000567684.2:n.129-94G>A
NM_000196.3:c.266-94G>A NP_000187.3:n.266-94G>A
NM_000196.4:c.266-94G>A MANE Select NP_000187.3:n.266-94G>A
Search 100 bp 5'
Search 100 bp 3'