Canonical Allele Identifier: CA587286368

Gene:

Linked Data

• dbSNP Id: rs1262645265
• gnomAD v2: 9-25551381-CT-C
• gnomAD v3: 9-25551383-CT-C
• gnomAD v4: 9-25551383-CT-C
• MyVariant Identifiers: chr9:g.25551382del (hg19) ; chr9:g.25551384del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551386del , CM000671.2:g.25551386del	GRCh38
NC_000009.11:g.25551384del , CM000671.1:g.25551384del	GRCh37
NC_000009.10:g.25541384del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-812del
XR_929525.2:n.674-812del