Canonical Allele Identifier: CA207989725

Gene:

Linked Data

• dbSNP Id: rs79224310
• gnomAD v2: 10-59572578-T-C
• gnomAD v3: 10-57812818-T-C
• gnomAD v4: 10-57812818-T-C
• MyVariant Identifiers: chr10:g.59572578T>C (hg19) ; chr10:g.57812818T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.57812818T>C , CM000672.2:g.57812818T>C	GRCh38
NC_000010.10:g.59572578T>C , CM000672.1:g.59572578T>C	GRCh37
NC_000010.9:g.59242584T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945979.1:n.68+34474A>G
XR_001747454.1:n.85+34474A>G