Canonical Allele Identifier: CA776019747
Gene:

Linked Data

dbSNP Id: rs1470085415
MyVariant Identifiers: chr18:g.10321299A>C (hg19) chr18:g.10321302A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321302A>C , CM000680.2:g.10321302A>C GRCh38
NC_000018.9:g.10321299A>C , CM000680.1:g.10321299A>C GRCh37
NC_000018.8:g.10311299A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+846T>G
XR_001753344.1:n.650+846T>G
XR_001753345.1:n.819T>G
XR_001753346.1:n.549+846T>G
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