Canonical Allele Identifier: CA805576773

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1426347329
• gnomAD v3: 5-150155822-G-T
• gnomAD v4: 5-150155822-G-T
• MyVariant Identifiers: chr5:g.149535385G>T (hg19) ; chr5:g.150155822G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155822G>T , CM000667.2:g.150155822G>T	GRCh38
NC_000005.9:g.149535385G>T , CM000667.1:g.149535385G>T	GRCh37
NC_000005.8:g.149515578G>T	NCBI36
NG_023367.1:g.5038C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-432C>A MANE Select	ENSP00000261799.4:n.-432C>A
ENST00000261799.8:c.-432C>A	ENSP00000261799.4:n.-432C>A
ENST00000517660.1:n.39C>A
ENST00000520579.5:c.-432C>A	ENSP00000430026.1:n.-432C>A
ENST00000523456.1:n.51C>A
NM_002609.3:c.-432C>A	NP_002600.1:n.-432C>A
XM_005268464.2:c.-578C>A	XP_005268521.1:n.-578C>A
XM_011537659.1:c.-899C>A	XP_011535961.1:n.-899C>A
NM_001355016.1:c.-578C>A	NP_001341945.1:n.-578C>A
NM_001355017.1:c.-949C>A	NP_001341946.1:n.-949C>A
NR_149150.1:n.38C>A
NM_002609.4:c.-432C>A MANE Select	NP_002600.1:n.-432C>A
NM_001355016.2:c.-578C>A	NP_001341945.1:n.-578C>A
NM_001355017.2:c.-949C>A	NP_001341946.1:n.-949C>A
NR_149150.2:n.24C>A