Canonical Allele Identifier: CA207989739

Gene:

Linked Data

• dbSNP Id: rs537849124
• gnomAD v2: 10-59572729-A-G
• gnomAD v3: 10-57812969-A-G
• gnomAD v4: 10-57812969-A-G
• MyVariant Identifiers: chr10:g.59572729A>G (hg19) ; chr10:g.57812969A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.57812969A>G , CM000672.2:g.57812969A>G	GRCh38
NC_000010.10:g.59572729A>G , CM000672.1:g.59572729A>G	GRCh37
NC_000010.9:g.59242735A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945979.1:n.68+34323T>C
XR_001747454.1:n.85+34323T>C