Canonical Allele Identifier: CA129082569
Gene: PDGFRB HGNC NCBI

Linked Data

dbSNP Id: rs113974960 rs2126600523 rs2126600532
gnomAD v2: 5-149535434-A-T
gnomAD v3: 5-150155871-A-T
gnomAD v4: 5-150155871-A-T
MyVariant Identifiers: chr5:g.149535434A>T (hg19) chr5:g.150155871A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155871A>T , CM000667.2:g.150155871A>T GRCh38
NC_000005.9:g.149535434A>T , CM000667.1:g.149535434A>T GRCh37
NC_000005.8:g.149515627A>T NCBI36
NG_023367.1:g.4989T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000523456.1:n.2T>A
XM_005268464.2:c.-627T>A XP_005268521.1:n.-627T>A
XM_011537659.1:c.-948T>A XP_011535961.1:n.-948T>A
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