Canonical Allele Identifier: CA2731720069
Gene:

Linked Data

dbSNP Id: rs2141420762

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249456del , CM000678.2:g.9249456del GRCh38
NC_000016.9:g.9343313del , CM000678.1:g.9343313del GRCh37
NC_000016.8:g.9250814del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64723del