Canonical Allele Identifier: CA2675968611

Gene: PDGFRB

Linked Data

• gnomAD v4: 5-150155779-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150155779C>G , CM000667.2:g.150155779C>G	GRCh38
NC_000005.9:g.149535342C>G , CM000667.1:g.149535342C>G	GRCh37
NC_000005.8:g.149515535C>G	NCBI36
NG_023367.1:g.5081G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261799.9:c.-389G>C MANE Select	ENSP00000261799.4:n.-389G>C
ENST00000261799.8:c.-389G>C	ENSP00000261799.4:n.-389G>C
ENST00000517660.1:n.82G>C
ENST00000520579.5:c.-389G>C	ENSP00000430026.1:n.-389G>C
ENST00000523456.1:n.94G>C
NM_002609.3:c.-389G>C	NP_002600.1:n.-389G>C
XM_005268464.2:c.-535G>C	XP_005268521.1:n.-535G>C
XM_011537659.1:c.-856G>C	XP_011535961.1:n.-856G>C
NM_001355016.1:c.-535G>C	NP_001341945.1:n.-535G>C
NM_001355017.1:c.-906G>C	NP_001341946.1:n.-906G>C
NR_149150.1:n.81G>C
NM_002609.4:c.-389G>C MANE Select	NP_002600.1:n.-389G>C
NM_001355016.2:c.-535G>C	NP_001341945.1:n.-535G>C
NM_001355017.2:c.-906G>C	NP_001341946.1:n.-906G>C
NR_149150.2:n.67G>C