Canonical Allele Identifier: CA1459814000
Gene: IGFBP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57046929G= , CM000666.2:g.57046929G= GRCh38
NC_000004.11:g.57913095G= , CM000666.1:g.57913095G= GRCh37
NC_000004.10:g.57607852G= NCBI36
NG_031877.1:g.68457C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295666.6:c.476-5996C= MANE Select ENSP00000295666.4:n.476-5996C=
ENST00000512512.3:n.116-5996C=
ENST00000514062.2:c.476-5996C= ENSP00000486293.1:n.476-5996C=
NM_001253835.1:c.476-5996C= NP_001240764.1:n.476-5996C=
NM_001553.2:c.476-5996C= NP_001544.1:n.476-5996C=
NM_001553.3:c.476-5996C= MANE Select NP_001544.1:n.476-5996C=
NM_001253835.2:c.476-5996C= NP_001240764.1:n.476-5996C=