Canonical Allele Identifier: CA3002196678
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762612del , CM000672.2:g.94762612del GRCh38
NC_000010.10:g.96522369del , CM000672.1:g.96522369del GRCh37
NC_000010.9:g.96512359del NCBI36
NG_008384.2:g.4907del
NG_008384.3:g.4932del

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12446del ENSP00000483243.1:n.932-12446del