Canonical Allele Identifier: CA10581725

Gene:

Linked Data

• ClinVar Variation Id: 240761
• ClinVar RCV Id: RCV000230316 ; RCV003982975
• dbSNP Id: rs183658182
• gnomAD v2: 1-15764902-C-T
• gnomAD v3: 1-15438406-C-T
• gnomAD v4: 1-15438406-C-T
• MyVariant Identifiers: chr1:g.15764902C>T (hg19) ; chr1:g.15438406C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15438406C>T , CM000663.2:g.15438406C>T	GRCh38
NC_000001.10:g.15764902C>T , CM000663.1:g.15764902C>T	GRCh37
NC_000001.9:g.15637489C>T	NCBI36
NG_009253.1:g.4965C>T