Canonical Allele Identifier: CA2656783598

Gene: PDGFB

Linked Data

• gnomAD v4: 22-39244739-AGCTGCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39244740_39244745del , CM000684.2:g.39244740_39244745del	GRCh38
NC_000022.10:g.39640745_39640750del , CM000684.1:g.39640745_39640750del	GRCh37
NC_000022.9:g.37970691_37970696del	NCBI36
NG_012111.1:g.5208_5213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331163.11:c.-782_-777del MANE Select	ENSP00000330382.6:n.-782_-777del
ENST00000331163.10:c.-782_-777del	ENSP00000330382.6:n.-782_-777del
NM_002608.2:c.-782_-777del	NP_002599.1:n.-782_-777del
NM_002608.3:c.-782_-777del	NP_002599.1:n.-782_-777del
NM_002608.4:c.-782_-777del MANE Select	NP_002599.1:n.-782_-777del