Canonical Allele Identifier: CA2405204834

Gene: PDGFB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39244592_39244618delinsGGCGGCGGGCACGGCTGCTCCGCGCGC , CM000684.2:g.39244592_39244618delinsGGCGGCGGGCACGGCTGCTCCGCGCGC	GRCh38
NC_000022.10:g.39640597_39640623delinsGGCGGCGGGCACGGCTGCTCCGCGCGC , CM000684.1:g.39640597_39640623delinsGGCGGCGGGCACGGCTGCTCCGCGCGC	GRCh37
NC_000022.9:g.37970543_37970569delinsGGCGGCGGGCACGGCTGCTCCGCGCGC	NCBI36
NG_012111.1:g.5335_5361delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331163.11:c.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC MANE Select	ENSP00000330382.6:n.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGC...
ENST00000331163.10:c.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC	ENSP00000330382.6:n.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGC...
NM_002608.2:c.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC	NP_002599.1:n.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC
NM_002608.3:c.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC	NP_002599.1:n.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC
NM_002608.4:c.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC MANE Select	NP_002599.1:n.-655_-629delinsGCGCGCGGAGCAGCCGTGCCCGCCGCC