Canonical Allele Identifier: CA2405204938
Gene: PDGFB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244732G= , CM000684.2:g.39244732G= GRCh38
NC_000022.10:g.39640737G= , CM000684.1:g.39640737G= GRCh37
NC_000022.9:g.37970683G= NCBI36
NG_012111.1:g.5221C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-769C= MANE Select ENSP00000330382.6:n.-769C=
ENST00000331163.10:c.-769C= ENSP00000330382.6:n.-769C=
NM_002608.2:c.-769C= NP_002599.1:n.-769C=
NM_002608.3:c.-769C= NP_002599.1:n.-769C=
NM_002608.4:c.-769C= MANE Select NP_002599.1:n.-769C=
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