Canonical Allele Identifier: CA628431496
Gene:

Linked Data

gnomAD v2: 18-10321341-TCCCAAAGG-T
MyVariant Identifiers: chr18:g.10321342_10321349del (hg19) chr18:g.10321345_10321352del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321345_10321352del , CM000680.2:g.10321345_10321352del GRCh38
NC_000018.9:g.10321342_10321349del , CM000680.1:g.10321342_10321349del GRCh37
NC_000018.8:g.10311342_10311349del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+796_665+803del
XR_001753344.1:n.650+796_650+803del
XR_001753345.1:n.769_776del
XR_001753346.1:n.549+796_549+803del
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