Canonical Allele Identifier: CA1459826051
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs1725115824

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57073523A>C , CM000666.2:g.57073523A>C GRCh38
NC_000004.11:g.57939689A>C , CM000666.1:g.57939689A>C GRCh37
NC_000004.10:g.57634446A>C NCBI36
NG_031877.1:g.41863T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295666.6:c.476-32590T>G MANE Select ENSP00000295666.4:n.476-32590T>G
ENST00000514062.2:c.476-32590T>G ENSP00000486293.1:n.476-32590T>G
NM_001253835.1:c.476-32590T>G NP_001240764.1:n.476-32590T>G
NM_001553.2:c.476-32590T>G NP_001544.1:n.476-32590T>G
NM_001553.3:c.476-32590T>G MANE Select NP_001544.1:n.476-32590T>G
NM_001253835.2:c.476-32590T>G NP_001240764.1:n.476-32590T>G