Canonical Allele Identifier: CA590667419

Gene:

Linked Data

• dbSNP Id: rs1374384451
• gnomAD v2: 9-132339100-CAG-C
• gnomAD v3: 9-129576821-CAG-C
• gnomAD v4: 9-129576821-CAG-C
• MyVariant Identifiers: chr9:g.132339101_132339102del (hg19) ; chr9:g.129576822_129576823del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576825_129576826del , CM000671.2:g.129576825_129576826del	GRCh38
NC_000009.11:g.132339104_132339105del , CM000671.1:g.132339104_132339105del	GRCh37
NC_000009.10:g.131378925_131378926del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1227_182+1228del