Canonical Allele Identifier: CA2675968617

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155784-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155784T>C , CM000667.2:g.150155784T>C	GRCh38
NC_000005.9:g.149535347T>C , CM000667.1:g.149535347T>C	GRCh37
NC_000005.8:g.149515540T>C	NCBI36
NG_023367.1:g.5076A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-394A>G MANE Select	ENSP00000261799.4:n.-394A>G
ENST00000261799.8:c.-394A>G	ENSP00000261799.4:n.-394A>G
ENST00000517660.1:n.77A>G
ENST00000520579.5:c.-394A>G	ENSP00000430026.1:n.-394A>G
ENST00000523456.1:n.89A>G
NM_002609.3:c.-394A>G	NP_002600.1:n.-394A>G
XM_005268464.2:c.-540A>G	XP_005268521.1:n.-540A>G
XM_011537659.1:c.-861A>G	XP_011535961.1:n.-861A>G
NM_001355016.1:c.-540A>G	NP_001341945.1:n.-540A>G
NM_001355017.1:c.-911A>G	NP_001341946.1:n.-911A>G
NR_149150.1:n.76A>G
NM_002609.4:c.-394A>G MANE Select	NP_002600.1:n.-394A>G
NM_001355016.2:c.-540A>G	NP_001341945.1:n.-540A>G
NM_001355017.2:c.-911A>G	NP_001341946.1:n.-911A>G
NR_149150.2:n.62A>G