Canonical Allele Identifier: CA107754150

Gene:

Linked Data

• dbSNP Id: rs909480436
• MyVariant Identifiers: chr4:g.145522762_145522767del (hg19) ; chr4:g.144601610_144601615del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601612_144601617del , CM000666.2:g.144601612_144601617del	GRCh38
NC_000004.11:g.145522764_145522769del , CM000666.1:g.145522764_145522769del	GRCh37
NC_000004.10:g.145742214_145742219del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649263.1:c.328-185637_328-185632del	ENSP00000497507.1:n.328-185637_328-185632...