Canonical Allele Identifier: CA880474132

Gene:

Linked Data

• dbSNP Id: rs1297067844
• MyVariant Identifiers: chr19:g.20217869_20217870insGTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217872_20217875dup , CM000681.2:g.20217872_20217875dup	GRCh38
NC_000019.9:g.20328681_20328684dup , CM000681.1:g.20328681_20328684dup	GRCh37
NC_000019.8:g.20189681_20189684dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-557_619-554dup
XR_936389.1:n.502-557_502-554dup
XR_936390.1:n.511-557_511-554dup
XR_936391.1:n.514-557_514-554dup
XR_936392.1:n.514-557_514-554dup
XR_936394.1:n.41-862_41-859dup
XR_001754063.2:n.1506-557_1506-554dup
XR_001754064.2:n.138-557_138-554dup
XR_001754066.1:n.3912-557_3912-554dup
XR_001754067.1:n.3912-557_3912-554dup
XR_001754068.1:n.3912-557_3912-554dup
XR_936394.2:n.41-862_41-859dup
XR_936406.2:n.1411-557_1411-554dup