Canonical Allele Identifier: CA666857969
Gene:

Linked Data

dbSNP Id: rs1188082097
MyVariant Identifiers: chr10:g.59572356A>G (hg19) chr10:g.57812596A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812596A>G , CM000672.2:g.57812596A>G GRCh38
NC_000010.10:g.59572356A>G , CM000672.1:g.59572356A>G GRCh37
NC_000010.9:g.59242362A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34696T>C
XR_001747454.1:n.85+34696T>C
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