Canonical Allele Identifier: CA1459826062
Gene: IGFBP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57073543T= , CM000666.2:g.57073543T= GRCh38
NC_000004.11:g.57939709T= , CM000666.1:g.57939709T= GRCh37
NC_000004.10:g.57634466T= NCBI36
NG_031877.1:g.41843A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295666.6:c.476-32610A= MANE Select ENSP00000295666.4:n.476-32610A=
ENST00000514062.2:c.476-32610A= ENSP00000486293.1:n.476-32610A=
NM_001253835.1:c.476-32610A= NP_001240764.1:n.476-32610A=
NM_001553.2:c.476-32610A= NP_001544.1:n.476-32610A=
NM_001553.3:c.476-32610A= MANE Select NP_001544.1:n.476-32610A=
NM_001253835.2:c.476-32610A= NP_001240764.1:n.476-32610A=