Canonical Allele Identifier: CA920077194

Gene:

Linked Data

• dbSNP Id: rs1599734219

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218419_20218420insCGGGG , CM000681.2:g.20218419_20218420insCGGGG	GRCh38
NC_000019.9:g.20329228_20329229insCGGGG , CM000681.1:g.20329228_20329229insCGGGG	GRCh37
NC_000019.8:g.20190228_20190229insCGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1104_619-1103insCCCCG
XR_936389.1:n.502-1104_502-1103insCCCCG
XR_936390.1:n.511-1104_511-1103insCCCCG
XR_936391.1:n.514-1104_514-1103insCCCCG
XR_936392.1:n.514-1104_514-1103insCCCCG
XR_936394.1:n.41-315_41-314insCGGGG
XR_001754063.2:n.1506-1104_1506-1103insCCCCG
XR_001754064.2:n.138-1104_138-1103insCCCCG
XR_001754066.1:n.3912-1104_3912-1103insCCCCG
XR_001754067.1:n.3912-1104_3912-1103insCCCCG
XR_001754068.1:n.3912-1104_3912-1103insCCCCG
XR_936394.2:n.41-315_41-314insCGGGG
XR_936406.2:n.1411-1104_1411-1103insCCCCG