Canonical Allele Identifier: CA629270353
Gene:

Linked Data

dbSNP Id: rs1281421779
gnomAD v2: 18-29336509-TC-T
gnomAD v3: 18-31756546-TC-T
gnomAD v4: 18-31756546-TC-T
MyVariant Identifiers: chr18:g.29336510del (hg19) chr18:g.31756547del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756549del , CM000680.2:g.31756549del GRCh38
NC_000018.9:g.29336512del , CM000680.1:g.29336512del GRCh37
NC_000018.8:g.27590510del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5590del
Search 100 bp 5'
Search 100 bp 3'