Canonical Allele Identifier: CA1481405925
Gene:

Linked Data

dbSNP Id: rs1738895909

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499999_102500000del , CM000666.2:g.102499999_102500000del GRCh38
NC_000004.11:g.103421156_103421157del , CM000666.1:g.103421156_103421157del GRCh37
NC_000004.10:g.103640188_103640189del NCBI36
NG_050628.1:g.3671_3672del

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1251_643+1252del XP_011530769.1:n.643+1251_643+1252del
NR_136202.1:n.48+2441_48+2442del