Canonical Allele Identifier: CA2633779651
Gene: HSD11B2 HGNC NCBI

Linked Data

gnomAD v4: 16-67436410-G-GGA
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436411_67436412insAG , CM000678.2:g.67436411_67436412insAG GRCh38
NC_000016.9:g.67470314_67470315insAG , CM000678.1:g.67470314_67470315insAG GRCh37
NC_000016.8:g.66027815_66027816insAG NCBI36
NG_011482.1:g.49776_49777insTC
NG_016549.1:g.10279_10280insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000326152.6:c.802+25_802+26insAG MANE Select ENSP00000316786.5:n.802+25_802+26insAG
ENST00000326152.5:c.802+25_802+26insAG ENSP00000316786.5:n.802+25_802+26insAG
NM_000196.3:c.802+25_802+26insAG NP_000187.3:n.802+25_802+26insAG
NM_000196.4:c.802+25_802+26insAG MANE Select NP_000187.3:n.802+25_802+26insAG
Search 100 bp 5'
Search 100 bp 3'