Canonical Allele Identifier: CA1025684082

Gene: PDGFB

Linked Data

• gnomAD v3: 22-39244801-CTTT-C
• gnomAD v4: 22-39244801-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39244815_39244817del , CM000684.2:g.39244815_39244817del	GRCh38
NC_000022.10:g.39640820_39640822del , CM000684.1:g.39640820_39640822del	GRCh37
NC_000022.9:g.37970766_37970768del	NCBI36
NG_012111.1:g.5149_5151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331163.11:c.-841_-839del MANE Select	ENSP00000330382.6:n.-841_-839del
NM_002608.2:c.-841_-839del	NP_002599.1:n.-841_-839del
NM_002608.3:c.-841_-839del	NP_002599.1:n.-841_-839del
NM_002608.4:c.-841_-839del MANE Select	NP_002599.1:n.-841_-839del