Canonical Allele Identifier: CA2700308939
Gene:

Linked Data

dbSNP Id: rs2104659752

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883942_122883943del , CM000664.2:g.122883942_122883943del GRCh38
NC_000002.11:g.123641518_123641519del , CM000664.1:g.123641518_123641519del GRCh37
NC_000002.10:g.123357988_123357989del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-1000_1125-999del
XR_001739692.1:n.1451-1000_1451-999del
XR_923292.2:n.1358-1000_1358-999del