Canonical Allele Identifier: CA1804794063
Gene:

Linked Data

dbSNP Id: rs1810396779

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269542_97269548del , CM000670.2:g.97269542_97269548del GRCh38
NC_000008.10:g.98281770_98281776del , CM000670.1:g.98281770_98281776del GRCh37
NC_000008.9:g.98350946_98350952del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149522_471+149528del