Canonical Allele Identifier: CA1804794089
Gene:

Linked Data

dbSNP Id: rs1810396970

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269552_97269555del , CM000670.2:g.97269552_97269555del GRCh38
NC_000008.10:g.98281780_98281783del , CM000670.1:g.98281780_98281783del GRCh37
NC_000008.9:g.98350956_98350959del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149515_471+149518del