Canonical Allele Identifier: CA158302423

Gene:

Linked Data

• dbSNP Id: rs907696401
• MyVariant Identifiers: chr7:g.46072642C>T (hg19) ; chr7:g.46033044C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.46033044C>T , CM000669.2:g.46033044C>T	GRCh38
NC_000007.13:g.46072642C>T , CM000669.1:g.46072642C>T	GRCh37
NC_000007.12:g.46039167C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745203.1:n.1270-3574C>T