Canonical Allele Identifier: CA2405204963
Gene: PDGFB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244753A= , CM000684.2:g.39244753A= GRCh38
NC_000022.10:g.39640758A= , CM000684.1:g.39640758A= GRCh37
NC_000022.9:g.37970704A= NCBI36
NG_012111.1:g.5200T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-790T= MANE Select ENSP00000330382.6:n.-790T=
NM_002608.2:c.-790T= NP_002599.1:n.-790T=
NM_002608.3:c.-790T= NP_002599.1:n.-790T=
NM_002608.4:c.-790T= MANE Select NP_002599.1:n.-790T=
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