Canonical Allele Identifier: CA207989713
Gene:

Linked Data

dbSNP Id: rs11591522
gnomAD v2: 10-59572511-G-A
gnomAD v3: 10-57812751-G-A
gnomAD v4: 10-57812751-G-A
MyVariant Identifiers: chr10:g.59572511G>A (hg19) chr10:g.57812751G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812751G>A , CM000672.2:g.57812751G>A GRCh38
NC_000010.10:g.59572511G>A , CM000672.1:g.59572511G>A GRCh37
NC_000010.9:g.59242517G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34541C>T
XR_001747454.1:n.85+34541C>T
Search 100 bp 5'
Search 100 bp 3'