Canonical Allele Identifier: CA805576775

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1245770260
• gnomAD v4: 5-150155826-G-A
• MyVariant Identifiers: chr5:g.149535389G>A (hg19) ; chr5:g.150155826G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155826G>A , CM000667.2:g.150155826G>A	GRCh38
NC_000005.9:g.149535389G>A , CM000667.1:g.149535389G>A	GRCh37
NC_000005.8:g.149515582G>A	NCBI36
NG_023367.1:g.5034C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-436C>T MANE Select	ENSP00000261799.4:n.-436C>T
ENST00000261799.8:c.-436C>T	ENSP00000261799.4:n.-436C>T
ENST00000517660.1:n.35C>T
ENST00000520579.5:c.-436C>T	ENSP00000430026.1:n.-436C>T
ENST00000523456.1:n.47C>T
NM_002609.3:c.-436C>T	NP_002600.1:n.-436C>T
XM_005268464.2:c.-582C>T	XP_005268521.1:n.-582C>T
XM_011537659.1:c.-903C>T	XP_011535961.1:n.-903C>T
NM_001355016.1:c.-582C>T	NP_001341945.1:n.-582C>T
NM_001355017.1:c.-953C>T	NP_001341946.1:n.-953C>T
NR_149150.1:n.34C>T
NM_002609.4:c.-436C>T MANE Select	NP_002600.1:n.-436C>T
NM_001355016.2:c.-582C>T	NP_001341945.1:n.-582C>T
NM_001355017.2:c.-953C>T	NP_001341946.1:n.-953C>T
NR_149150.2:n.20C>T