Canonical Allele Identifier: CA1459814001
Gene: IGFBP7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57046930A= , CM000666.2:g.57046930A= GRCh38
NC_000004.11:g.57913096A= , CM000666.1:g.57913096A= GRCh37
NC_000004.10:g.57607853A= NCBI36
NG_031877.1:g.68456T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295666.6:c.476-5997T= MANE Select ENSP00000295666.4:n.476-5997T=
ENST00000512512.3:n.116-5997T=
ENST00000514062.2:c.476-5997T= ENSP00000486293.1:n.476-5997T=
NM_001253835.1:c.476-5997T= NP_001240764.1:n.476-5997T=
NM_001553.2:c.476-5997T= NP_001544.1:n.476-5997T=
NM_001553.3:c.476-5997T= MANE Select NP_001544.1:n.476-5997T=
NM_001253835.2:c.476-5997T= NP_001240764.1:n.476-5997T=
Search 100 bp 5'
Search 100 bp 3'