Canonical Allele Identifier: CA1687324634
Gene:

Linked Data

dbSNP Id: rs1782267867

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816862del , CM000669.2:g.9816862del GRCh38
NC_000007.13:g.9856491del , CM000669.1:g.9856491del GRCh37
NC_000007.12:g.9823016del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+49928del
XR_927025.1:n.323+49928del
XR_927026.1:n.209+49928del
XR_927026.2:n.209+49928del