Canonical Allele Identifier: CA880474179
Gene:

Linked Data

dbSNP Id: rs1160731256
MyVariant Identifiers: chr19:g.20217889del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217891del , CM000681.2:g.20217891del GRCh38
NC_000019.9:g.20328700del , CM000681.1:g.20328700del GRCh37
NC_000019.8:g.20189700del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-573del
XR_936389.1:n.502-573del
XR_936390.1:n.511-573del
XR_936391.1:n.514-573del
XR_936392.1:n.514-573del
XR_936394.1:n.41-843del
XR_001754063.2:n.1506-573del
XR_001754064.2:n.138-573del
XR_001754066.1:n.3912-573del
XR_001754067.1:n.3912-573del
XR_001754068.1:n.3912-573del
XR_936394.2:n.41-843del
XR_936406.2:n.1411-573del