Canonical Allele Identifier: CA207989695
Gene:

Linked Data

dbSNP Id: rs564240515
gnomAD v3: 10-57812589-C-A
gnomAD v4: 10-57812589-C-A
MyVariant Identifiers: chr10:g.59572349C>A (hg19) chr10:g.57812589C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812589C>A , CM000672.2:g.57812589C>A GRCh38
NC_000010.10:g.59572349C>A , CM000672.1:g.59572349C>A GRCh37
NC_000010.9:g.59242355C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34703G>T
XR_001747454.1:n.85+34703G>T
Search 100 bp 5'
Search 100 bp 3'