Canonical Allele Identifier: CA563560808

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1467581880
• gnomAD v2: 5-149535398-T-C
• gnomAD v3: 5-150155835-T-C
• gnomAD v4: 5-150155835-T-C
• MyVariant Identifiers: chr5:g.149535398T>C (hg19) ; chr5:g.150155835T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155835T>C , CM000667.2:g.150155835T>C	GRCh38
NC_000005.9:g.149535398T>C , CM000667.1:g.149535398T>C	GRCh37
NC_000005.8:g.149515591T>C	NCBI36
NG_023367.1:g.5025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-445A>G MANE Select	ENSP00000261799.4:n.-445A>G
ENST00000261799.8:c.-445A>G	ENSP00000261799.4:n.-445A>G
ENST00000517660.1:n.26A>G
ENST00000520579.5:c.-445A>G	ENSP00000430026.1:n.-445A>G
ENST00000523456.1:n.38A>G
NM_002609.3:c.-445A>G	NP_002600.1:n.-445A>G
XM_005268464.2:c.-591A>G	XP_005268521.1:n.-591A>G
XM_011537659.1:c.-912A>G	XP_011535961.1:n.-912A>G
NM_001355016.1:c.-591A>G	NP_001341945.1:n.-591A>G
NM_001355017.1:c.-962A>G	NP_001341946.1:n.-962A>G
NR_149150.1:n.25A>G
NM_002609.4:c.-445A>G MANE Select	NP_002600.1:n.-445A>G
NM_001355016.2:c.-591A>G	NP_001341945.1:n.-591A>G
NM_001355017.2:c.-962A>G	NP_001341946.1:n.-962A>G
NR_149150.2:n.11A>G