Canonical Allele Identifier: CA181547494

Gene:

Linked Data

• dbSNP Id: rs540040919
• gnomAD v3: 8-88535625-CA-C
• gnomAD v4: 8-88535625-CA-C
• MyVariant Identifiers: chr8:g.89547855del (hg19) ; chr8:g.88535626del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88535626del , CM000670.2:g.88535626del	GRCh38
NC_000008.10:g.89547855del , CM000670.1:g.89547855del	GRCh37
NC_000008.9:g.89616971del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745651.2:n.1673+10891del
XR_001745653.2:n.286-7054del
XR_928383.3:n.1475+10891del