Canonical Allele Identifier: CA797158705

Gene:

Linked Data

• dbSNP Id: rs774563694
• MyVariant Identifiers: chr4:g.63423969C>G (hg19) ; chr4:g.62558251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558251C>G , CM000666.2:g.62558251C>G	GRCh38
NC_000004.11:g.63423969C>G , CM000666.1:g.63423969C>G	GRCh37
NC_000004.10:g.63106564C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5593C>G