Canonical Allele Identifier: CA797158679

Gene:

Linked Data

• dbSNP Id: rs1430776889
• MyVariant Identifiers: chr4:g.63423937C>T (hg19) ; chr4:g.62558219C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558219C>T , CM000666.2:g.62558219C>T	GRCh38
NC_000004.11:g.63423937C>T , CM000666.1:g.63423937C>T	GRCh37
NC_000004.10:g.63106532C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5625C>T