Canonical Allele Identifier: CA97647895
Gene: IGFBP7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs114518130

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57047087G>A , CM000666.2:g.57047087G>A GRCh38
NC_000004.11:g.57913253G>A , CM000666.1:g.57913253G>A GRCh37
NC_000004.10:g.57608010G>A NCBI36
NG_031877.1:g.68299C>T

Transcript Alleles

HGVS Amino-acid change
NM_001253835.1:c.476-6154C>T VV NP_001240764.1:p.=
NM_001553.2:c.476-6154C>T VV NP_001544.1:p.=
NM_001553.3:c.476-6154C>T VV MANE Preferred NP_001544.1:p.=
ENST00000295666.6:c.476-6154C>T ENSP00000295666.4:p.=
ENST00000512512.3:n.116-6154C>T
ENST00000514062.2:c.476-6154C>T ENSP00000486293.1:p.=