Canonical Allele Identifier: CA472023470
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI
IGF2-AS HGNC NCBI

Linked Data

dbSNP Id: rs756466104
gnomAD v2: 11-2167627-G-T
gnomAD v3: 11-2146397-G-T
gnomAD v4: 11-2146397-G-T
MyVariant Identifiers: chr11:g.2167627G>T (hg19) chr11:g.2146397G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146397G>T , CM000673.2:g.2146397G>T GRCh38
NC_000011.9:g.2167627G>T , CM000673.1:g.2167627G>T GRCh37
NC_000011.8:g.2124203G>T NCBI36
NG_008849.1:g.8207C>A
NG_050578.1:g.19813C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1169C>A (IGF2) ENSP00000511998.1:n.-7+1169C>A
ENST00000643349.2:c.*46+1169C>A ENSP00000495715.1:n.*46+1169C>A
ENST00000695541.1:c.-7+1169C>A (IGF2) ENSP00000511997.1:n.-7+1169C>A
ENST00000643349.1:c.*46+1169C>A ENSP00000495715.1:n.*46+1169C>A
ENST00000356578.8:c.*46+1169C>A (INS-IGF2) ENSP00000348986.4:n.*46+1169C>A
NM_001007139.5:c.-7+1169C>A (IGF2) NP_001007140.2:n.-7+1169C>A
NR_003512.3:n.708+1169C>A (INS-IGF2)
NR_028043.2:n.589G>T (IGF2-AS)
NR_133657.1:n.478G>T (IGF2-AS)
NR_003512.4:n.708+1169C>A (INS-IGF2)
NM_001007139.6:c.-7+1169C>A (IGF2) NP_001007140.2:n.-7+1169C>A
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