Canonical Allele Identifier: CA2580100530
Gene:

Linked Data

ClinVar Variation Id: 10974
ClinVar RCV Id: RCV000011721
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304157_30306387delinsTGGAAATTATATATATTTCCAAATAAA , CM000685.2:g.30304157_30306387delinsTGGAAATTATATATATTTCCAAATAAA GRCh38
NC_000023.10:g.30322274_30324504delinsTGGAAATTATATATATTTCCAAATAAA , CM000685.1:g.30322274_30324504delinsTGGAAATTATATATATTTCCAAATAAA GRCh37
NC_000023.9:g.30232195_30234425delinsTGGAAATTATATATATTTCCAAATAAA NCBI36
NG_009814.1:g.7992_10222delinsTTTATTTGGAAATATATATAATTTCCA
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