Canonical Allele Identifier: CA920369865
Gene: PDGFB HGNC NCBI

Linked Data

dbSNP Id: rs71326753

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244746_39244759dup , CM000684.2:g.39244746_39244759dup GRCh38
NC_000022.10:g.39640751_39640764dup , CM000684.1:g.39640751_39640764dup GRCh37
NC_000022.9:g.37970697_37970710dup NCBI36
NG_012111.1:g.5207_5220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-783_-770dup MANE Select ENSP00000330382.6:n.-783_-770dup
NM_002608.2:c.-783_-770dup NP_002599.1:n.-783_-770dup
NM_002608.3:c.-783_-770dup NP_002599.1:n.-783_-770dup
NM_002608.4:c.-783_-770dup MANE Select NP_002599.1:n.-783_-770dup