Canonical Allele Identifier: CA740538642

Gene:

Linked Data

• dbSNP Id: rs1303355274
• MyVariant Identifiers: chr1:g.95029606C>T (hg19) ; chr1:g.94564050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94564050C>T , CM000663.2:g.94564050C>T	GRCh38
NC_000001.10:g.95029606C>T , CM000663.1:g.95029606C>T	GRCh37
NC_000001.9:g.94802194C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738161.1:n.461+437C>T