Canonical Allele Identifier: CA1931617863
Gene:

Linked Data

dbSNP Id: rs2041646213

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101681del , CM000672.2:g.100101681del GRCh38
NC_000010.10:g.101861438del , CM000672.1:g.101861438del GRCh37
NC_000010.9:g.101851428del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5444del