Canonical Allele Identifier: CA271505104
Gene:

Linked Data

ClinVar Variation Id: 1257483
ClinVar RCV Id: RCV001668747
dbSNP Id: rs58967026
gnomAD v2: 15-65322166-CTTTA-C
gnomAD v3: 15-65029828-CTTTA-C
gnomAD v4: 15-65029828-CTTTA-C
MyVariant Identifiers: chr15:g.65322167_65322170del (hg19) chr15:g.65029829_65029832del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65029860_65029863del , CM000677.2:g.65029860_65029863del GRCh38
NC_000015.9:g.65322198_65322201del , CM000677.1:g.65322198_65322201del GRCh37
NC_000015.8:g.63109251_63109254del NCBI36
NG_029184.1:g.4808_4811del
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