Canonical Allele Identifier: CA163327781
Gene:

Linked Data

ClinVar Variation Id: 13572
ClinVar RCV Id: RCV000014540
dbSNP Id: rs1799762
gnomAD v2: 7-100769706-T-TG
gnomAD v3: 7-101126425-T-TG
gnomAD v4: 7-101126425-T-TG
MyVariant Identifiers: chr7:g.100769706_100769707insG (hg19) chr7:g.101126425_101126426insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.101126429dup , CM000669.2:g.101126429dup GRCh38
NC_000007.13:g.100769710dup , CM000669.1:g.100769710dup GRCh37
NC_000007.12:g.100556430dup NCBI36
NG_013213.1:g.4332dup , LRG_597:g.4332dup
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