Canonical Allele Identifier: CA593764906

Gene:

Linked Data

• dbSNP Id: rs1160328706
• gnomAD v2: 10-59572598-A-T
• gnomAD v3: 10-57812838-A-T
• gnomAD v4: 10-57812838-A-T
• MyVariant Identifiers: chr10:g.59572598A>T (hg19) ; chr10:g.57812838A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.57812838A>T , CM000672.2:g.57812838A>T	GRCh38
NC_000010.10:g.59572598A>T , CM000672.1:g.59572598A>T	GRCh37
NC_000010.9:g.59242604A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945979.1:n.68+34454T>A
XR_001747454.1:n.85+34454T>A