Canonical Allele Identifier: CA191701705

Gene:

Linked Data

• dbSNP Id: rs552175020
• gnomAD v2: 9-25551411-AT-A
• gnomAD v3: 9-25551413-AT-A
• gnomAD v4: 9-25551413-AT-A
• MyVariant Identifiers: chr9:g.25551412del (hg19) ; chr9:g.25551414del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551414del , CM000671.2:g.25551414del	GRCh38
NC_000009.11:g.25551412del , CM000671.1:g.25551412del	GRCh37
NC_000009.10:g.25541412del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-842del
XR_929525.2:n.674-842del