Canonical Allele Identifier: CA296576136
Gene:

Linked Data

dbSNP Id: rs1027112929
MyVariant Identifiers: chr18:g.10382803T>C (hg19) chr18:g.10382806T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382806T>C , CM000680.2:g.10382806T>C GRCh38
NC_000018.9:g.10382803T>C , CM000680.1:g.10382803T>C GRCh37
NC_000018.8:g.10372803T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1453T>C
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