Canonical Allele Identifier: CA2695196467
Gene: PDGFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244732_39244739delinsGGCTGCGA , CM000684.2:g.39244732_39244739delinsGGCTGCGA GRCh38
NC_000022.10:g.39640737_39640744delinsGGCTGCGA , CM000684.1:g.39640737_39640744delinsGGCTGCGA GRCh37
NC_000022.9:g.37970683_37970690delinsGGCTGCGA NCBI36
NG_012111.1:g.5214_5221delinsTCGCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-776_-769delinsTCGCAGCC MANE Select ENSP00000330382.6:n.-776_-769delinsTCGCAGCC
ENST00000331163.10:c.-776_-769delinsTCGCAGCC ENSP00000330382.6:n.-776_-769delinsTCGCAGCC
NM_002608.2:c.-776_-769delinsTCGCAGCC NP_002599.1:n.-776_-769delinsTCGCAGCC
NM_002608.3:c.-776_-769delinsTCGCAGCC NP_002599.1:n.-776_-769delinsTCGCAGCC
NM_002608.4:c.-776_-769delinsTCGCAGCC MANE Select NP_002599.1:n.-776_-769delinsTCGCAGCC