Canonical Allele Identifier: CA2656783628
Gene: PDGFB HGNC NCBI

Linked Data

gnomAD v4: 22-39244796-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39244796G>T , CM000684.2:g.39244796G>T GRCh38
NC_000022.10:g.39640801G>T , CM000684.1:g.39640801G>T GRCh37
NC_000022.9:g.37970747G>T NCBI36
NG_012111.1:g.5157C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331163.11:c.-833C>A MANE Select ENSP00000330382.6:n.-833C>A
NM_002608.2:c.-833C>A NP_002599.1:n.-833C>A
NM_002608.3:c.-833C>A NP_002599.1:n.-833C>A
NM_002608.4:c.-833C>A MANE Select NP_002599.1:n.-833C>A
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Search 100 bp 3'