Canonical Allele Identifier: CA596378549
Gene:

Linked Data

dbSNP Id: rs1439410673
gnomAD v2: 10-124217848-TG-T
gnomAD v3: 10-122458332-TG-T
gnomAD v4: 10-122458332-TG-T
MyVariant Identifiers: chr10:g.124217849del (hg19) chr10:g.122458333del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458333del , CM000672.2:g.122458333del GRCh38
NC_000010.10:g.124217849del , CM000672.1:g.124217849del GRCh37
NC_000010.9:g.124207839del NCBI36
NG_011554.1:g.1809del
NG_011725.1:g.8671del

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+162del
XR_946383.1:n.1827+162del
XR_946384.1:n.1576+162del
XR_946385.1:n.1827+162del
XR_946382.2:n.1855+162del
XR_946383.2:n.1855+162del
XR_946384.2:n.1580+162del
XR_946385.2:n.1855+162del
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