Canonical Allele Identifier: CA97656284
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs1026493899
MyVariant Identifiers: chr4:g.57939707G>A (hg19) chr4:g.57073541G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57073541G>A , CM000666.2:g.57073541G>A GRCh38
NC_000004.11:g.57939707G>A , CM000666.1:g.57939707G>A GRCh37
NC_000004.10:g.57634464G>A NCBI36
NG_031877.1:g.41845C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295666.6:c.476-32608C>T MANE Select ENSP00000295666.4:n.476-32608C>T
ENST00000514062.2:c.476-32608C>T ENSP00000486293.1:n.476-32608C>T
NM_001253835.1:c.476-32608C>T NP_001240764.1:n.476-32608C>T
NM_001553.2:c.476-32608C>T NP_001544.1:n.476-32608C>T
NM_001553.3:c.476-32608C>T MANE Select NP_001544.1:n.476-32608C>T
NM_001253835.2:c.476-32608C>T NP_001240764.1:n.476-32608C>T
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