Canonical Allele Identifier: CA1931617870
Gene:

Linked Data

dbSNP Id: rs2041646252

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101699del , CM000672.2:g.100101699del GRCh38
NC_000010.10:g.101861456del , CM000672.1:g.101861456del GRCh37
NC_000010.9:g.101851446del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5462del