Canonical Allele Identifier: CA129082561
Gene: PDGFRB HGNC NCBI

Linked Data

dbSNP Id: rs897619719
gnomAD v3: 5-150155860-C-T
gnomAD v4: 5-150155860-C-T
MyVariant Identifiers: chr5:g.149535423C>T (hg19) chr5:g.150155860C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155860C>T , CM000667.2:g.150155860C>T GRCh38
NC_000005.9:g.149535423C>T , CM000667.1:g.149535423C>T GRCh37
NC_000005.8:g.149515616C>T NCBI36
NG_023367.1:g.5000G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261799.8:c.-470G>A ENSP00000261799.4:n.-470G>A
ENST00000517660.1:n.1G>A
ENST00000523456.1:n.13G>A
XM_005268464.2:c.-616G>A XP_005268521.1:n.-616G>A
XM_011537659.1:c.-937G>A XP_011535961.1:n.-937G>A
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