Canonical Allele Identifier: CA786695548

Gene:

Linked Data

• dbSNP Id: rs1208157318
• MyVariant Identifiers: chr4:g.12579842_12579843del (hg19) ; chr4:g.12578218_12578219del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12578224_12578225del , CM000666.2:g.12578224_12578225del	GRCh38
NC_000004.11:g.12579848_12579849del , CM000666.1:g.12579848_12579849del	GRCh37
NC_000004.10:g.12188946_12188947del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_925406.1:n.106+31123_106+31124del
XR_001741374.1:n.254+44436_254+44437del
XR_925406.3:n.140+31123_140+31124del