Canonical Allele Identifier: CA98367556

Gene:

Linked Data

• dbSNP Id: rs981728790
• MyVariant Identifiers: chr4:g.63423857A>G (hg19) ; chr4:g.62558139A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558139A>G , CM000666.2:g.62558139A>G	GRCh38
NC_000004.11:g.63423857A>G , CM000666.1:g.63423857A>G	GRCh37
NC_000004.10:g.63106452A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5705A>G