Canonical Allele Identifier: CA735235299
Gene:

Linked Data

dbSNP Id: rs1322601627
gnomAD v3: 1-34523558-G-GT
gnomAD v4: 1-34523558-G-GT
MyVariant Identifiers: chr1:g.34989159_34989160insT (hg19) chr1:g.34523558_34523559insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523559dup , CM000663.2:g.34523559dup GRCh38
NC_000001.10:g.34989160dup , CM000663.1:g.34989160dup GRCh37
NC_000001.9:g.34761747dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24020dup
XR_001737964.1:n.991+24020dup
Search 100 bp 5'
Search 100 bp 3'