Canonical Allele Identifier: CA632705491

Gene:

Linked Data

• dbSNP Id: rs1568518249
• gnomAD v2: 19-34012868-TG-T
• gnomAD v3: 19-33521962-TG-T
• gnomAD v4: 19-33521962-TG-T
• MyVariant Identifiers: chr19:g.34012869del (hg19) ; chr19:g.33521963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521967del , CM000681.2:g.33521967del	GRCh38
NC_000019.9:g.34012873del , CM000681.1:g.34012873del	GRCh37
NC_000019.8:g.38704713del	NCBI36
NG_013358.1:g.4931del
NG_013358.2:g.4931del

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.26del
XR_935919.1:n.21del
XR_001754035.2:n.34del
XR_935918.2:n.34del