Canonical Allele Identifier: CA910080446
Gene:

Linked Data

dbSNP Id: rs1236248862
MyVariant Identifiers: chr3:g.72315970_72315975del (hg19) chr3:g.72266819_72266824del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266819_72266824del , CM000665.2:g.72266819_72266824del GRCh38
NC_000003.11:g.72315970_72315975del , CM000665.1:g.72315970_72315975del GRCh37
NC_000003.10:g.72398660_72398665del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8284_835+8289del
Search 100 bp 5'
Search 100 bp 3'