Canonical Allele Identifier: CA296568464
Gene:

Linked Data

dbSNP Id: rs182135344
gnomAD v3: 18-10321380-T-A
gnomAD v4: 18-10321380-T-A
MyVariant Identifiers: chr18:g.10321377T>A (hg19) chr18:g.10321380T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321380T>A , CM000680.2:g.10321380T>A GRCh38
NC_000018.9:g.10321377T>A , CM000680.1:g.10321377T>A GRCh37
NC_000018.8:g.10311377T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935138.1:n.665+768A>T
XR_001753344.1:n.650+768A>T
XR_001753345.1:n.741A>T
XR_001753346.1:n.549+768A>T
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