Canonical Allele Identifier: CA666857961
Gene:

Linked Data

dbSNP Id: rs995037938
MyVariant Identifiers: chr10:g.59572346A>C (hg19) chr10:g.57812586A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812586A>C , CM000672.2:g.57812586A>C GRCh38
NC_000010.10:g.59572346A>C , CM000672.1:g.59572346A>C GRCh37
NC_000010.9:g.59242352A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34706T>G
XR_001747454.1:n.85+34706T>G
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