Canonical Allele Identifier: CA833583486
Gene:

Linked Data

dbSNP Id: rs1198121125
MyVariant Identifiers: chr7:g.13440274_13440275insACTCTGCT (hg19) chr7:g.13400649_13400650insACTCTGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400654_13400655insGCTACTCT , CM000669.2:g.13400654_13400655insGCTACTCT GRCh38
NC_000007.13:g.13440279_13440280insGCTACTCT , CM000669.1:g.13440279_13440280insGCTACTCT GRCh37
NC_000007.12:g.13406804_13406805insGCTACTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90331_147+90332insGCTACTCT
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