Canonical Allele Identifier: CA796557887
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs1271138532
MyVariant Identifiers: chr4:g.57913250A>C (hg19) chr4:g.57047084A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57047084A>C , CM000666.2:g.57047084A>C GRCh38
NC_000004.11:g.57913250A>C , CM000666.1:g.57913250A>C GRCh37
NC_000004.10:g.57608007A>C NCBI36
NG_031877.1:g.68302T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295666.6:c.476-6151T>G MANE Select ENSP00000295666.4:n.476-6151T>G
ENST00000512512.3:n.116-6151T>G
ENST00000514062.2:c.476-6151T>G ENSP00000486293.1:n.476-6151T>G
NM_001253835.1:c.476-6151T>G NP_001240764.1:n.476-6151T>G
NM_001553.2:c.476-6151T>G NP_001544.1:n.476-6151T>G
NM_001553.3:c.476-6151T>G MANE Select NP_001544.1:n.476-6151T>G
NM_001253835.2:c.476-6151T>G NP_001240764.1:n.476-6151T>G
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