Canonical Allele Identifier: CA298296897
Gene:

Linked Data

dbSNP Id: rs962947645
gnomAD v2: 18-29336982-T-TTTTA
gnomAD v3: 18-31757019-T-TTTTA
gnomAD v4: 18-31757019-T-TTTTA
MyVariant Identifiers: chr18:g.29336982_29336983insTTTA (hg19) chr18:g.31757019_31757020insTTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757035_31757038dup , CM000680.2:g.31757035_31757038dup GRCh38
NC_000018.9:g.29336998_29337001dup , CM000680.1:g.29336998_29337001dup GRCh37
NC_000018.8:g.27590996_27590999dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5104_66-5101dup
Search 100 bp 5'
Search 100 bp 3'