Canonical Allele Identifier: CA805576772

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1157600493
• gnomAD v3: 5-150155817-G-T
• gnomAD v4: 5-150155817-G-T
• MyVariant Identifiers: chr5:g.149535380G>T (hg19) ; chr5:g.150155817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155817G>T , CM000667.2:g.150155817G>T	GRCh38
NC_000005.9:g.149535380G>T , CM000667.1:g.149535380G>T	GRCh37
NC_000005.8:g.149515573G>T	NCBI36
NG_023367.1:g.5043C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-427C>A MANE Select	ENSP00000261799.4:n.-427C>A
ENST00000261799.8:c.-427C>A	ENSP00000261799.4:n.-427C>A
ENST00000517660.1:n.44C>A
ENST00000520579.5:c.-427C>A	ENSP00000430026.1:n.-427C>A
ENST00000523456.1:n.56C>A
NM_002609.3:c.-427C>A	NP_002600.1:n.-427C>A
XM_005268464.2:c.-573C>A	XP_005268521.1:n.-573C>A
XM_011537659.1:c.-894C>A	XP_011535961.1:n.-894C>A
NM_001355016.1:c.-573C>A	NP_001341945.1:n.-573C>A
NM_001355017.1:c.-944C>A	NP_001341946.1:n.-944C>A
NR_149150.1:n.43C>A
NM_002609.4:c.-427C>A MANE Select	NP_002600.1:n.-427C>A
NM_001355016.2:c.-573C>A	NP_001341945.1:n.-573C>A
NM_001355017.2:c.-944C>A	NP_001341946.1:n.-944C>A
NR_149150.2:n.29C>A