Canonical Allele Identifier: CA207989702
Gene:

Linked Data

dbSNP Id: rs758009426
gnomAD v2: 10-59572417-G-A
gnomAD v3: 10-57812657-G-A
gnomAD v4: 10-57812657-G-A
MyVariant Identifiers: chr10:g.59572417G>A (hg19) chr10:g.57812657G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812657G>A , CM000672.2:g.57812657G>A GRCh38
NC_000010.10:g.59572417G>A , CM000672.1:g.59572417G>A GRCh37
NC_000010.9:g.59242423G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34635C>T
XR_001747454.1:n.85+34635C>T
Search 100 bp 5'
Search 100 bp 3'