Canonical Allele Identifier: CA144319793
Gene:

Linked Data

dbSNP Id: rs955843689
gnomAD v2: 6-98550379-C-CT
gnomAD v3: 6-98102503-C-CT
gnomAD v4: 6-98102503-C-CT
MyVariant Identifiers: chr6:g.98550380_98550381insT (hg19) chr6:g.98550379_98550380insT (hg19) chr6:g.98102504_98102505insT (hg38) chr6:g.98102503_98102504insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102512dup , CM000668.2:g.98102512dup GRCh38
NC_000006.11:g.98550388dup , CM000668.1:g.98550388dup GRCh37
NC_000006.10:g.98657109dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3242dup
XR_942809.1:n.456+3242dup
Search 100 bp 5'
Search 100 bp 3'