Canonical Allele Identifier: CA2605389662

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1580828760
• gnomAD v3: 5-150155812-T-A
• gnomAD v4: 5-150155812-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155812T>A , CM000667.2:g.150155812T>A	GRCh38
NC_000005.9:g.149535375T>A , CM000667.1:g.149535375T>A	GRCh37
NC_000005.8:g.149515568T>A	NCBI36
NG_023367.1:g.5048A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-422A>T MANE Select	ENSP00000261799.4:n.-422A>T
ENST00000261799.8:c.-422A>T	ENSP00000261799.4:n.-422A>T
ENST00000517660.1:n.49A>T
ENST00000520579.5:c.-422A>T	ENSP00000430026.1:n.-422A>T
ENST00000523456.1:n.61A>T
NM_002609.3:c.-422A>T	NP_002600.1:n.-422A>T
XM_005268464.2:c.-568A>T	XP_005268521.1:n.-568A>T
XM_011537659.1:c.-889A>T	XP_011535961.1:n.-889A>T
NM_001355016.1:c.-568A>T	NP_001341945.1:n.-568A>T
NM_001355017.1:c.-939A>T	NP_001341946.1:n.-939A>T
NR_149150.1:n.48A>T
NM_002609.4:c.-422A>T MANE Select	NP_002600.1:n.-422A>T
NM_001355016.2:c.-568A>T	NP_001341945.1:n.-568A>T
NM_001355017.2:c.-939A>T	NP_001341946.1:n.-939A>T
NR_149150.2:n.34A>T