Canonical Allele Identifier: CA880474168

Gene:

Linked Data

• dbSNP Id: rs1423841893
• MyVariant Identifiers: chr19:g.20217881_20217882del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217881_20217882del , CM000681.2:g.20217881_20217882del	GRCh38
NC_000019.9:g.20328690_20328691del , CM000681.1:g.20328690_20328691del	GRCh37
NC_000019.8:g.20189690_20189691del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-566_619-565del
XR_936389.1:n.502-566_502-565del
XR_936390.1:n.511-566_511-565del
XR_936391.1:n.514-566_514-565del
XR_936392.1:n.514-566_514-565del
XR_936394.1:n.41-853_41-852del
XR_001754063.2:n.1506-566_1506-565del
XR_001754064.2:n.138-566_138-565del
XR_001754066.1:n.3912-566_3912-565del
XR_001754067.1:n.3912-566_3912-565del
XR_001754068.1:n.3912-566_3912-565del
XR_936394.2:n.41-853_41-852del
XR_936406.2:n.1411-566_1411-565del