Canonical Allele Identifier: CA1459826145
Gene: IGFBP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57073682A= , CM000666.2:g.57073682A= GRCh38
NC_000004.11:g.57939848A= , CM000666.1:g.57939848A= GRCh37
NC_000004.10:g.57634605A= NCBI36
NG_031877.1:g.41704T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295666.6:c.476-32749T= MANE Select ENSP00000295666.4:n.476-32749T=
ENST00000514062.2:c.476-32749T= ENSP00000486293.1:n.476-32749T=
NM_001253835.1:c.476-32749T= NP_001240764.1:n.476-32749T=
NM_001553.2:c.476-32749T= NP_001544.1:n.476-32749T=
NM_001553.3:c.476-32749T= MANE Select NP_001544.1:n.476-32749T=
NM_001253835.2:c.476-32749T= NP_001240764.1:n.476-32749T=