Canonical Allele Identifier: CA880474452

Gene:

Linked Data

• dbSNP Id: rs1277868675
• gnomAD v3: 19-20218367-GGGTGC-G
• gnomAD v4: 19-20218367-GGGTGC-G
• MyVariant Identifiers: chr19:g.20218368_20218372del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218372_20218376del , CM000681.2:g.20218372_20218376del	GRCh38
NC_000019.9:g.20329181_20329185del , CM000681.1:g.20329181_20329185del	GRCh37
NC_000019.8:g.20190181_20190185del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1056_619-1052del
XR_936389.1:n.502-1056_502-1052del
XR_936390.1:n.511-1056_511-1052del
XR_936391.1:n.514-1056_514-1052del
XR_936392.1:n.514-1056_514-1052del
XR_936394.1:n.41-362_41-358del
XR_001754063.2:n.1506-1056_1506-1052del
XR_001754064.2:n.138-1056_138-1052del
XR_001754066.1:n.3912-1056_3912-1052del
XR_001754067.1:n.3912-1056_3912-1052del
XR_001754068.1:n.3912-1056_3912-1052del
XR_936394.2:n.41-362_41-358del
XR_936406.2:n.1411-1056_1411-1052del