Canonical Allele Identifier: CA1704466872

Gene: IGFBP3

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45915430A>T , CM000669.2:g.45915430A>T	GRCh38
NC_000007.13:g.45955029A>T , CM000669.1:g.45955029A>T	GRCh37
NC_000007.12:g.45921554A>T	NCBI36
NG_011508.1:g.10843T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613132.5:c.751-485T>A MANE Select	ENSP00000477772.2:n.751-485T>A
ENST00000381083.9:c.769-485T>A	ENSP00000370473.4:n.769-485T>A
ENST00000275521.10:c.751-485T>A	ENSP00000275521.5:n.751-485T>A
ENST00000381083.8:c.769-485T>A	ENSP00000370473.4:n.769-485T>A
ENST00000381086.9:c.460-485T>A	ENSP00000370476.4:n.460-485T>A
ENST00000417621.5:c.335-485T>A
ENST00000428530.5:c.306-485T>A
ENST00000613132.4:c.688-485T>A	ENSP00000477772.1:n.688-485T>A
ENST00000615754.4:c.667-485T>A	ENSP00000480717.1:n.667-485T>A
NM_000598.4:c.751-485T>A	NP_000589.2:n.751-485T>A
NM_001013398.1:c.769-485T>A	NP_001013416.1:n.769-485T>A
NM_001013398.2:c.769-485T>A	NP_001013416.1:n.769-485T>A
NM_000598.5:c.751-485T>A MANE Select	NP_000589.2:n.751-485T>A