Canonical Allele Identifier: CA551778560
Gene: IGFBP7 HGNC NCBI

Linked Data

dbSNP Id: rs1271816673
gnomAD v2: 4-57913095-G-C
gnomAD v3: 4-57046929-G-C
gnomAD v4: 4-57046929-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.57046929G>C , CM000666.2:g.57046929G>C GRCh38
NC_000004.11:g.57913095G>C , CM000666.1:g.57913095G>C GRCh37
NC_000004.10:g.57607852G>C NCBI36
NG_031877.1:g.68457C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295666.6:c.476-5996C>G MANE Select ENSP00000295666.4:n.476-5996C>G
ENST00000512512.3:n.116-5996C>G
ENST00000514062.2:c.476-5996C>G ENSP00000486293.1:n.476-5996C>G
NM_001253835.1:c.476-5996C>G NP_001240764.1:n.476-5996C>G
NM_001553.2:c.476-5996C>G NP_001544.1:n.476-5996C>G
NM_001553.3:c.476-5996C>G MANE Select NP_001544.1:n.476-5996C>G
NM_001253835.2:c.476-5996C>G NP_001240764.1:n.476-5996C>G