Canonical Allele Identifier: CA633314786

Gene:

Linked Data

• dbSNP Id: rs747519137
• gnomAD v2: 19-45412778-C-CT
• gnomAD v3: 19-44909521-C-CT
• gnomAD v4: 19-44909521-C-CT
• MyVariant Identifiers: chr19:g.45412781_45412782insT (hg19) ; chr19:g.45412778_45412779insT (hg19) ; chr19:g.44909524_44909525insT (hg38) ; chr19:g.44909521_44909522insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909535dup , CM000681.2:g.44909535dup	GRCh38
NC_000019.9:g.45412792dup , CM000681.1:g.45412792dup	GRCh37
NC_000019.8:g.50104632dup	NCBI36
NG_007084.2:g.8754dup