Canonical Allele Identifier: CA207989697
Gene:

Linked Data

dbSNP Id: rs528209792
MyVariant Identifiers: chr10:g.59572351C>G (hg19) chr10:g.57812591C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812591C>G , CM000672.2:g.57812591C>G GRCh38
NC_000010.10:g.59572351C>G , CM000672.1:g.59572351C>G GRCh37
NC_000010.9:g.59242357C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34701G>C
XR_001747454.1:n.85+34701G>C
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