Canonical Allele Identifier: CA857362234

Gene:

Linked Data

• dbSNP Id: rs1299765681
• gnomAD v3: 8-97269749-TG-T
• gnomAD v4: 8-97269749-TG-T
• MyVariant Identifiers: chr8:g.98281978del (hg19) ; chr8:g.97269750del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269752del , CM000670.2:g.97269752del	GRCh38
NC_000008.10:g.98281980del , CM000670.1:g.98281980del	GRCh37
NC_000008.9:g.98351156del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149320del