Canonical Allele Identifier: CA129082564
Gene: PDGFRB HGNC NCBI

Linked Data

dbSNP Id: rs933057448 rs2150537381
gnomAD v2: 5-149535432-C-T
gnomAD v3: 5-150155869-C-T
gnomAD v4: 5-150155869-C-T
MyVariant Identifiers: chr5:g.149535432C>T (hg19) chr5:g.150155869C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155869C>T , CM000667.2:g.150155869C>T GRCh38
NC_000005.9:g.149535432C>T , CM000667.1:g.149535432C>T GRCh37
NC_000005.8:g.149515625C>T NCBI36
NG_023367.1:g.4991G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000523456.1:n.4G>A
XM_005268464.2:c.-625G>A XP_005268521.1:n.-625G>A
XM_011537659.1:c.-946G>A XP_011535961.1:n.-946G>A
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