Canonical Allele Identifier: CA2327233174
Gene:

Linked Data

dbSNP Id: rs2090128274

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218218del , CM000681.2:g.20218218del GRCh38
NC_000019.9:g.20329027del , CM000681.1:g.20329027del GRCh37
NC_000019.8:g.20190027del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936388.1:n.619-901del
XR_936389.1:n.502-901del
XR_936390.1:n.511-901del
XR_936391.1:n.514-901del
XR_936392.1:n.514-901del
XR_936394.1:n.41-516del
XR_001754063.2:n.1506-901del
XR_001754064.2:n.138-901del
XR_001754066.1:n.3912-901del
XR_001754067.1:n.3912-901del
XR_001754068.1:n.3912-901del
XR_936394.2:n.41-516del
XR_936406.2:n.1411-901del