Canonical Allele Identifier: CA74805333

Gene:

Linked Data

• dbSNP Id: rs756628944
• MyVariant Identifiers: chr3:g.53091213_53091217del (hg19) ; chr3:g.53057197_53057201del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53057200_53057204del , CM000665.2:g.53057200_53057204del	GRCh38
NC_000003.11:g.53091216_53091220del , CM000665.1:g.53091216_53091220del	GRCh37
NC_000003.10:g.53066256_53066260del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607203.1:c.318-9962_318-9958del
ENST00000607283.5:c.465-13947_465-13943del
ENST00000607495.5:c.447+20487_447+20491del