Canonical Allele Identifier: CA506174776

Gene:

Linked Data

• dbSNP Id: rs532385427
• MyVariant Identifiers: chr19:g.20328750_20328752del (hg19) ; chr19:g.20217941_20217943del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217942_20217944del , CM000681.2:g.20217942_20217944del	GRCh38
NC_000019.9:g.20328751_20328753del , CM000681.1:g.20328751_20328753del	GRCh37
NC_000019.8:g.20189751_20189753del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-627_619-625del
XR_936389.1:n.502-627_502-625del
XR_936390.1:n.511-627_511-625del
XR_936391.1:n.514-627_514-625del
XR_936392.1:n.514-627_514-625del
XR_936394.1:n.41-792_41-790del
XR_001754063.2:n.1506-627_1506-625del
XR_001754064.2:n.138-627_138-625del
XR_001754066.1:n.3912-627_3912-625del
XR_001754067.1:n.3912-627_3912-625del
XR_001754068.1:n.3912-627_3912-625del
XR_936394.2:n.41-792_41-790del
XR_936406.2:n.1411-627_1411-625del