Canonical Allele Identifier: CA920077193

Gene:

Linked Data

• dbSNP Id: rs1599734210

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218418_20218419insGGGGGGG , CM000681.2:g.20218418_20218419insGGGGGGG	GRCh38
NC_000019.9:g.20329227_20329228insGGGGGGG , CM000681.1:g.20329227_20329228insGGGGGGG	GRCh37
NC_000019.8:g.20190227_20190228insGGGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1100_619-1099insCCCCCCC
XR_936389.1:n.502-1100_502-1099insCCCCCCC
XR_936390.1:n.511-1100_511-1099insCCCCCCC
XR_936391.1:n.514-1100_514-1099insCCCCCCC
XR_936392.1:n.514-1100_514-1099insCCCCCCC
XR_936394.1:n.41-316_41-315insGGGGGGG
XR_001754063.2:n.1506-1100_1506-1099insCCCCCCC
XR_001754064.2:n.138-1100_138-1099insCCCCCCC
XR_001754066.1:n.3912-1100_3912-1099insCCCCCCC
XR_001754067.1:n.3912-1100_3912-1099insCCCCCCC
XR_001754068.1:n.3912-1100_3912-1099insCCCCCCC
XR_936394.2:n.41-316_41-315insGGGGGGG
XR_936406.2:n.1411-1100_1411-1099insCCCCCCC