Canonical Allele Identifier: CA1284674092
Gene:

Linked Data

dbSNP Id: rs1680372099

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883916_122883919del , CM000664.2:g.122883916_122883919del GRCh38
NC_000002.11:g.123641492_123641495del , CM000664.1:g.123641492_123641495del GRCh37
NC_000002.10:g.123357962_123357965del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1026_1125-1023del
XR_001739692.1:n.1451-1026_1451-1023del
XR_923292.2:n.1358-1026_1358-1023del