Canonical Allele Identifier: CA207989723
Gene:

Linked Data

dbSNP Id: rs1031442035
gnomAD v2: 10-59572555-G-C
gnomAD v3: 10-57812795-G-C
gnomAD v4: 10-57812795-G-C
MyVariant Identifiers: chr10:g.59572555G>C (hg19) chr10:g.57812795G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812795G>C , CM000672.2:g.57812795G>C GRCh38
NC_000010.10:g.59572555G>C , CM000672.1:g.59572555G>C GRCh37
NC_000010.9:g.59242561G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34497C>G
XR_001747454.1:n.85+34497C>G
Search 100 bp 5'
Search 100 bp 3'