Canonical Allele Identifier: CA2656783640
Gene: PDGFB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244804_39244805insG , CM000684.2:g.39244804_39244805insG GRCh38
NC_000022.10:g.39640809_39640810insG , CM000684.1:g.39640809_39640810insG GRCh37
NC_000022.9:g.37970755_37970756insG NCBI36
NG_012111.1:g.5148_5149insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-842_-841insC MANE Select ENSP00000330382.6:n.-842_-841insC
NM_002608.2:c.-842_-841insC NP_002599.1:n.-842_-841insC
NM_002608.3:c.-842_-841insC NP_002599.1:n.-842_-841insC
NM_002608.4:c.-842_-841insC MANE Select NP_002599.1:n.-842_-841insC