Canonical Allele Identifier: CA674543782
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI
IGF2-AS HGNC NCBI

Linked Data

dbSNP Id: rs1272768511
gnomAD v3: 11-2146046-G-C
gnomAD v4: 11-2146046-G-C
MyVariant Identifiers: chr11:g.2167276G>C (hg19) chr11:g.2146046G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146046G>C , CM000673.2:g.2146046G>C GRCh38
NC_000011.9:g.2167276G>C , CM000673.1:g.2167276G>C GRCh37
NC_000011.8:g.2123852G>C NCBI36
NG_008849.1:g.8558C>G
NG_050578.1:g.20164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-7+1520C>G (IGF2) ENSP00000511998.1:n.-7+1520C>G
ENST00000643349.2:c.*46+1520C>G ENSP00000495715.1:n.*46+1520C>G
ENST00000695541.1:c.-7+1520C>G (IGF2) ENSP00000511997.1:n.-7+1520C>G
ENST00000643349.1:c.*46+1520C>G ENSP00000495715.1:n.*46+1520C>G
ENST00000356578.8:c.*46+1520C>G (INS-IGF2) ENSP00000348986.4:n.*46+1520C>G
NM_001007139.5:c.-7+1520C>G (IGF2) NP_001007140.2:n.-7+1520C>G
NR_003512.3:n.708+1520C>G (INS-IGF2)
NR_028043.2:n.437-199G>C (IGF2-AS)
NR_133657.1:n.437-310G>C (IGF2-AS)
NR_003512.4:n.708+1520C>G (INS-IGF2)
NM_001007139.6:c.-7+1520C>G (IGF2) NP_001007140.2:n.-7+1520C>G
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