Canonical Allele Identifier: CA97647799
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs958285134
gnomAD v2: 4-57913094-A-G
gnomAD v3: 4-57046928-A-G
gnomAD v4: 4-57046928-A-G
MyVariant Identifiers: chr4:g.57913094A>G (hg19) chr4:g.57046928A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57046928A>G , CM000666.2:g.57046928A>G GRCh38
NC_000004.11:g.57913094A>G , CM000666.1:g.57913094A>G GRCh37
NC_000004.10:g.57607851A>G NCBI36
NG_031877.1:g.68458T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295666.6:c.476-5995T>C MANE Select ENSP00000295666.4:n.476-5995T>C
ENST00000512512.3:n.116-5995T>C
ENST00000514062.2:c.476-5995T>C ENSP00000486293.1:n.476-5995T>C
NM_001253835.1:c.476-5995T>C NP_001240764.1:n.476-5995T>C
NM_001553.2:c.476-5995T>C NP_001544.1:n.476-5995T>C
NM_001553.3:c.476-5995T>C MANE Select NP_001544.1:n.476-5995T>C
NM_001253835.2:c.476-5995T>C NP_001240764.1:n.476-5995T>C
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