Canonical Allele Identifier: CA779336987

Gene:

Linked Data

• dbSNP Id: rs1256343959
• gnomAD v3: 18-41477799-G-GA
• gnomAD v4: 18-41477799-G-GA
• MyVariant Identifiers: chr18:g.39057763_39057764insA (hg19) ; chr18:g.41477799_41477800insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477801dup , CM000680.2:g.41477801dup	GRCh38
NC_000018.9:g.39057765dup , CM000680.1:g.39057765dup	GRCh37
NC_000018.8:g.37311763dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26333dup