Canonical Allele Identifier: CA1062849338
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs1724382681
gnomAD v3: 4-57047145-T-C
gnomAD v4: 4-57047145-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57047145T>C , CM000666.2:g.57047145T>C GRCh38
NC_000004.11:g.57913311T>C , CM000666.1:g.57913311T>C GRCh37
NC_000004.10:g.57608068T>C NCBI36
NG_031877.1:g.68241A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295666.6:c.476-6212A>G MANE Select ENSP00000295666.4:n.476-6212A>G
ENST00000512512.3:n.116-6212A>G
ENST00000514062.2:c.476-6212A>G ENSP00000486293.1:n.476-6212A>G
NM_001253835.1:c.476-6212A>G NP_001240764.1:n.476-6212A>G
NM_001553.2:c.476-6212A>G NP_001544.1:n.476-6212A>G
NM_001553.3:c.476-6212A>G MANE Select NP_001544.1:n.476-6212A>G
NM_001253835.2:c.476-6212A>G NP_001240764.1:n.476-6212A>G