Canonical Allele Identifier: CA296568462
Gene:

Linked Data

dbSNP Id: rs921387554
MyVariant Identifiers: chr18:g.10321376C>G (hg19) chr18:g.10321379C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321379C>G , CM000680.2:g.10321379C>G GRCh38
NC_000018.9:g.10321376C>G , CM000680.1:g.10321376C>G GRCh37
NC_000018.8:g.10311376C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935138.1:n.665+769G>C
XR_001753344.1:n.650+769G>C
XR_001753345.1:n.742G>C
XR_001753346.1:n.549+769G>C
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