Canonical Allele Identifier: CA666858074

Gene:

Linked Data

• dbSNP Id: rs1425403698
• gnomAD v3: 10-57812931-T-C
• gnomAD v4: 10-57812931-T-C
• MyVariant Identifiers: chr10:g.59572691T>C (hg19) ; chr10:g.57812931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.57812931T>C , CM000672.2:g.57812931T>C	GRCh38
NC_000010.10:g.59572691T>C , CM000672.1:g.59572691T>C	GRCh37
NC_000010.9:g.59242697T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945979.1:n.68+34361A>G
XR_001747454.1:n.85+34361A>G