Canonical Allele Identifier: CA2656783591
Gene: PDGFB HGNC NCBI

Linked Data

dbSNP Id: rs2146460507
gnomAD v4: 22-39244735-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244735T>C , CM000684.2:g.39244735T>C GRCh38
NC_000022.10:g.39640740T>C , CM000684.1:g.39640740T>C GRCh37
NC_000022.9:g.37970686T>C NCBI36
NG_012111.1:g.5218A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-772A>G MANE Select ENSP00000330382.6:n.-772A>G
ENST00000331163.10:c.-772A>G ENSP00000330382.6:n.-772A>G
NM_002608.2:c.-772A>G NP_002599.1:n.-772A>G
NM_002608.3:c.-772A>G NP_002599.1:n.-772A>G
NM_002608.4:c.-772A>G MANE Select NP_002599.1:n.-772A>G
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