Canonical Allele Identifier: CA805576792
Gene: PDGFRB HGNC NCBI

Linked Data

dbSNP Id: rs1217252007
gnomAD v3: 5-150155870-T-A
gnomAD v4: 5-150155870-T-A
MyVariant Identifiers: chr5:g.149535433T>A (hg19) chr5:g.150155870T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150155870T>A , CM000667.2:g.150155870T>A GRCh38
NC_000005.9:g.149535433T>A , CM000667.1:g.149535433T>A GRCh37
NC_000005.8:g.149515626T>A NCBI36
NG_023367.1:g.4990A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000523456.1:n.3A>T
XM_005268464.2:c.-626A>T XP_005268521.1:n.-626A>T
XM_011537659.1:c.-947A>T XP_011535961.1:n.-947A>T
Search 100 bp 5'
Search 100 bp 3'