Canonical Allele Identifier: CA797158587

Gene:

Linked Data

• dbSNP Id: rs1009346899
• MyVariant Identifiers: chr4:g.63423810del (hg19) ; chr4:g.62558092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558095del , CM000666.2:g.62558095del	GRCh38
NC_000004.11:g.63423813del , CM000666.1:g.63423813del	GRCh37
NC_000004.10:g.63106408del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5749del