Canonical Allele Identifier: CA97647817

Gene: IGFBP7

Linked Data

• dbSNP Id: rs369461339
• MyVariant Identifiers: chr4:g.57913150T>C (hg19) ; chr4:g.57046984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.57046984T>C , CM000666.2:g.57046984T>C	GRCh38
NC_000004.11:g.57913150T>C , CM000666.1:g.57913150T>C	GRCh37
NC_000004.10:g.57607907T>C	NCBI36
NG_031877.1:g.68402A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295666.6:c.476-6051A>G MANE Select	ENSP00000295666.4:n.476-6051A>G
ENST00000512512.3:n.116-6051A>G
ENST00000514062.2:c.476-6051A>G	ENSP00000486293.1:n.476-6051A>G
NM_001253835.1:c.476-6051A>G	NP_001240764.1:n.476-6051A>G
NM_001553.2:c.476-6051A>G	NP_001544.1:n.476-6051A>G
NM_001553.3:c.476-6051A>G MANE Select	NP_001544.1:n.476-6051A>G
NM_001253835.2:c.476-6051A>G	NP_001240764.1:n.476-6051A>G