Canonical Allele Identifier: CA915944145
Gene:

Linked Data

ClinVar Variation Id: 642168
ClinVar RCV Id: RCV000795578
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7582933_7587670delinsAGAGAAGAACAGTCTT , CM000668.2:g.7582933_7587670delinsAGAGAAGAACAGTCTT GRCh38
NC_000006.11:g.7583166_7587903delinsAGAGAAGAACAGTCTT , CM000668.1:g.7583166_7587903delinsAGAGAAGAACAGTCTT GRCh37
NC_000006.10:g.7528165_7532902delinsAGAGAAGAACAGTCTT NCBI36
NG_008803.1:g.46297_51034delinsAGAGAAGAACAGTCTT , LRG_423:g.46297_51034delinsAGAGAAGAACAGTCTT
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