Canonical Allele Identifier: CA857362216
Gene:

Linked Data

dbSNP Id: rs1246805520
MyVariant Identifiers: chr8:g.98281932_98281934del (hg19) chr8:g.97269704_97269706del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269707_97269709del , CM000670.2:g.97269707_97269709del GRCh38
NC_000008.10:g.98281935_98281937del , CM000670.1:g.98281935_98281937del GRCh37
NC_000008.9:g.98351111_98351113del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149364_471+149366del
Search 100 bp 5'
Search 100 bp 3'