Canonical Allele Identifier: CA805578987

Gene: PDGFRB

Linked Data

• dbSNP Id: rs1202490846
• gnomAD v3: 5-150120826-G-A
• gnomAD v4: 5-150120826-G-A
• MyVariant Identifiers: chr5:g.149500389G>A (hg19) ; chr5:g.150120826G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150120826G>A , CM000667.2:g.150120826G>A	GRCh38
NC_000005.9:g.149500389G>A , CM000667.1:g.149500389G>A	GRCh37
NC_000005.8:g.149480582G>A	NCBI36
NG_023367.1:g.40034C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261799.9:c.2586+62C>T MANE Select	ENSP00000261799.4:n.2586+62C>T
ENST00000261799.8:c.2586+62C>T	ENSP00000261799.4:n.2586+62C>T
ENST00000519575.5:n.500+62C>T
ENST00000520579.5:c.*1900+62C>T	ENSP00000430026.1:n.*1900+62C>T
NM_002609.3:c.2586+62C>T	NP_002600.1:n.2586+62C>T
XM_005268464.2:c.2394+62C>T	XP_005268521.1:n.2394+62C>T
XM_011537658.1:c.2586+62C>T	XP_011535960.1:n.2586+62C>T
XM_011537659.1:c.2586+62C>T	XP_011535961.1:n.2586+62C>T
XM_011537660.1:c.2586+62C>T	XP_011535962.1:n.2586+62C>T
NM_001355016.1:c.2394+62C>T	NP_001341945.1:n.2394+62C>T
NM_001355017.1:c.2103+62C>T	NP_001341946.1:n.2103+62C>T
NM_002609.4:c.2586+62C>T MANE Select	NP_002600.1:n.2586+62C>T
NM_001355016.2:c.2394+62C>T	NP_001341945.1:n.2394+62C>T
NM_001355017.2:c.2103+62C>T	NP_001341946.1:n.2103+62C>T