Canonical Allele Identifier: CA15653309
Gene:

Linked Data

dbSNP Id: rs7909889
gnomAD v2: 10-59572370-C-T
gnomAD v3: 10-57812610-C-T
gnomAD v4: 10-57812610-C-T
MyVariant Identifiers: chr10:g.59572370C>T (hg19) chr10:g.57812610C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812610C>T , CM000672.2:g.57812610C>T GRCh38
NC_000010.10:g.59572370C>T , CM000672.1:g.59572370C>T GRCh37
NC_000010.9:g.59242376C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34682G>A
XR_001747454.1:n.85+34682G>A
Search 100 bp 5'
Search 100 bp 3'