Canonical Allele Identifier: CA569191041
Gene:

Linked Data

dbSNP Id: rs34104748
gnomAD v2: 6-98550328-C-CTT
gnomAD v3: 6-98102452-C-CTT
gnomAD v4: 6-98102452-C-CTT
MyVariant Identifiers: chr6:g.98550329_98550330insTT (hg19) chr6:g.98550328_98550329insTT (hg19) chr6:g.98102453_98102454insTT (hg38) chr6:g.98102452_98102453insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102460_98102461dup , CM000668.2:g.98102460_98102461dup GRCh38
NC_000006.11:g.98550336_98550337dup , CM000668.1:g.98550336_98550337dup GRCh37
NC_000006.10:g.98657057_98657058dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3190_456+3191dup
XR_942809.1:n.456+3190_456+3191dup
Search 100 bp 5'
Search 100 bp 3'