Canonical Allele Identifier: CA619268023
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1318618298
gnomAD v2: 15-80883864-CG-C
gnomAD v3: 15-80591523-CG-C
gnomAD v4: 15-80591523-CG-C
MyVariant Identifiers: chr15:g.80883865del (hg19) chr15:g.80591524del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591526del , CM000677.2:g.80591526del GRCh38
NC_000015.9:g.80883867del , CM000677.1:g.80883867del GRCh37
NC_000015.8:g.78670922del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1919-42del MANE Select ENSP00000307479.4:n.1919-42del
ENST00000303329.8:c.1919-42del ENSP00000307479.4:n.1919-42del
ENST00000527771.5:c.1886-42del ENSP00000453792.1:n.1886-42del
ENST00000533983.5:c.1886-42del ENSP00000453651.1:n.1886-42del
ENST00000610490.4:c.*217-42del ENSP00000483762.1:n.*217-42del
ENST00000622346.4:c.1919-42del ENSP00000479393.1:n.1919-42del
NM_014862.3:c.1919-42del NP_055677.3:n.1919-42del
NM_014862.4:c.1919-42del MANE Select NP_055677.3:n.1919-42del
Search 100 bp 5'
Search 100 bp 3'