Canonical Allele Identifier: CA797158431

Gene:

Linked Data

• dbSNP Id: rs1164408852
• MyVariant Identifiers: chr4:g.63423561C>G (hg19) ; chr4:g.62557843C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62557843C>G , CM000666.2:g.62557843C>G	GRCh38
NC_000004.11:g.63423561C>G , CM000666.1:g.63423561C>G	GRCh37
NC_000004.10:g.63106156C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-6001C>G