Canonical Allele Identifier: CA308886512
Gene:

Linked Data

ClinVar Variation Id: 1287640
ClinVar RCV Id: RCV001710767
dbSNP Id: rs747519137
gnomAD v2: 19-45412778-CT-C
gnomAD v3: 19-44909521-CT-C
gnomAD v4: 19-44909521-CT-C
MyVariant Identifiers: chr19:g.45412781del (hg19) chr19:g.45412779del (hg19) chr19:g.44909524del (hg38) chr19:g.44909522del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909535del , CM000681.2:g.44909535del GRCh38
NC_000019.9:g.45412792del , CM000681.1:g.45412792del GRCh37
NC_000019.8:g.50104632del NCBI36
NG_007084.2:g.8754del
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