Canonical Allele Identifier: CA585052429
Gene:

Linked Data

dbSNP Id: rs1489502185
gnomAD v2: 8-128011778-TTATATG-T
gnomAD v3: 8-126999533-TTATATG-T
gnomAD v4: 8-126999533-TTATATG-T
MyVariant Identifiers: chr8:g.128011779_128011784del (hg19) chr8:g.126999534_126999539del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999538_126999543del , CM000670.2:g.126999538_126999543del GRCh38
NC_000008.10:g.128011783_128011788del , CM000670.1:g.128011783_128011788del GRCh37
NC_000008.9:g.128080965_128080970del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7017_1301-7012del
Search 100 bp 5'
Search 100 bp 3'