Canonical Allele Identifier: CA917712218
Gene:

Linked Data

dbSNP Id: rs1554240074

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440120del , CM000668.2:g.31440120del GRCh38
NC_000006.11:g.31407897del , CM000668.1:g.31407897del GRCh37
NC_000006.10:g.31515876del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-68del