Canonical Allele Identifier: CA98367546

Gene:

Linked Data

• dbSNP Id: rs914961781
• MyVariant Identifiers: chr4:g.63423820C>T (hg19) ; chr4:g.62558102C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558102C>T , CM000666.2:g.62558102C>T	GRCh38
NC_000004.11:g.63423820C>T , CM000666.1:g.63423820C>T	GRCh37
NC_000004.10:g.63106415C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5742C>T