Canonical Allele Identifier: CA881625360

Gene:

Linked Data

• dbSNP Id: rs1403980819
• gnomAD v3: 19-33521970-C-CA
• gnomAD v4: 19-33521970-C-CA
• MyVariant Identifiers: chr19:g.34012876_34012877insA (hg19) ; chr19:g.33521970_33521971insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521972dup , CM000681.2:g.33521972dup	GRCh38
NC_000019.9:g.34012878dup , CM000681.1:g.34012878dup	GRCh37
NC_000019.8:g.38704718dup	NCBI36
NG_013358.1:g.4923dup
NG_013358.2:g.4923dup

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.31dup
XR_935919.1:n.26dup
XR_001754035.2:n.39dup
XR_935918.2:n.39dup