Canonical Allele Identifier: CA593764902
Gene:

Linked Data

dbSNP Id: rs1235044861
gnomAD v2: 10-59572467-A-G
gnomAD v3: 10-57812707-A-G
gnomAD v4: 10-57812707-A-G
MyVariant Identifiers: chr10:g.59572467A>G (hg19) chr10:g.57812707A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812707A>G , CM000672.2:g.57812707A>G GRCh38
NC_000010.10:g.59572467A>G , CM000672.1:g.59572467A>G GRCh37
NC_000010.9:g.59242473A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34585T>C
XR_001747454.1:n.85+34585T>C
Search 100 bp 5'
Search 100 bp 3'