Canonical Allele Identifier: CA778454359
Gene:

Linked Data

dbSNP Id: rs1185624159
gnomAD v3: 18-31757013-TTTTTA-T
gnomAD v4: 18-31757013-TTTTTA-T
MyVariant Identifiers: chr18:g.29336977_29336981del (hg19) chr18:g.31757014_31757018del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757022_31757026del , CM000680.2:g.31757022_31757026del GRCh38
NC_000018.9:g.29336985_29336989del , CM000680.1:g.29336985_29336989del GRCh37
NC_000018.8:g.27590983_27590987del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5117_66-5113del
Search 100 bp 5'
Search 100 bp 3'