Canonical Allele Identifier: CA2405204962
Gene: PDGFB HGNC NCBI

Linked Data

dbSNP Id: rs1932654578

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244752G>A , CM000684.2:g.39244752G>A GRCh38
NC_000022.10:g.39640757G>A , CM000684.1:g.39640757G>A GRCh37
NC_000022.9:g.37970703G>A NCBI36
NG_012111.1:g.5201C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-789C>T MANE Select ENSP00000330382.6:n.-789C>T
NM_002608.2:c.-789C>T NP_002599.1:n.-789C>T
NM_002608.3:c.-789C>T NP_002599.1:n.-789C>T
NM_002608.4:c.-789C>T MANE Select NP_002599.1:n.-789C>T