Canonical Allele Identifier: CA798354201

Gene:

Linked Data

• dbSNP Id: rs1415509266
• MyVariant Identifiers: chr4:g.75170146_75170147del (hg19) ; chr4:g.74304429_74304430del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304432_74304433del , CM000666.2:g.74304432_74304433del	GRCh38
NC_000004.11:g.75170149_75170150del , CM000666.1:g.75170149_75170150del	GRCh37
NC_000004.10:g.75389013_75389014del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25652_120-25651del
XR_938877.2:n.126-25652_126-25651del