Canonical Allele Identifier: CA20757690

Gene:

Linked Data

• dbSNP Id: rs969067965
• gnomAD v3: 1-34523656-C-T
• gnomAD v4: 1-34523656-C-T
• MyVariant Identifiers: chr1:g.34989257C>T (hg19) ; chr1:g.34523656C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.34523656C>T , CM000663.2:g.34523656C>T	GRCh38
NC_000001.10:g.34989257C>T , CM000663.1:g.34989257C>T	GRCh37
NC_000001.9:g.34761844C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947171.1:n.1073+23923G>A
XR_001737964.1:n.991+23923G>A