Canonical Allele Identifier: CA3507337
Gene: PDGFRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150115724G>C , CM000667.2:g.150115724G>C GRCh38
NC_000005.9:g.149495287G>C , CM000667.1:g.149495287G>C GRCh37
NC_000005.8:g.149475480G>C NCBI36
NG_012303.1:g.2649C>G
NG_023367.1:g.45136C>G
NG_012303.2:g.2649C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.9:c.*39C>G MANE Select ENSP00000261799.4:n.*39C>G
ENST00000261799.8:c.*39C>G ENSP00000261799.4:n.*39C>G
NM_002609.3:c.*39C>G NP_002600.1:n.*39C>G
XM_005268464.2:c.*39C>G XP_005268521.1:n.*39C>G
XM_011537658.1:c.*39C>G XP_011535960.1:n.*39C>G
XM_011537659.1:c.*39C>G XP_011535961.1:n.*39C>G
NM_001355016.1:c.*39C>G NP_001341945.1:n.*39C>G
NM_001355017.1:c.*39C>G NP_001341946.1:n.*39C>G
NM_002609.4:c.*39C>G MANE Select NP_002600.1:n.*39C>G
NM_001355016.2:c.*39C>G NP_001341945.1:n.*39C>G
NM_001355017.2:c.*39C>G NP_001341946.1:n.*39C>G