Canonical Allele Identifier: CA1948014998

Linked Data

dbSNP Id: rs1260056115

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2146069C>A , CM000673.2:g.2146069C>A GRCh38
NC_000011.9:g.2167299C>A , CM000673.1:g.2167299C>A GRCh37
NC_000011.8:g.2123875C>A NCBI36
NG_008849.1:g.8535G>T
NG_050578.1:g.20141G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.-7+1497G>T (IGF2) ENSP00000511998.1:n.-7+1497G>T
ENST00000643349.2:c.*46+1497G>T ENSP00000495715.1:n.*46+1497G>T
ENST00000695541.1:c.-7+1497G>T (IGF2) ENSP00000511997.1:n.-7+1497G>T
ENST00000643349.1:c.*46+1497G>T ENSP00000495715.1:n.*46+1497G>T
ENST00000356578.8:c.*46+1497G>T (INS-IGF2) ENSP00000348986.4:n.*46+1497G>T
NM_001007139.5:c.-7+1497G>T (IGF2) NP_001007140.2:n.-7+1497G>T
NR_003512.3:n.708+1497G>T (INS-IGF2)
NR_028043.2:n.437-176C>A (IGF2-AS)
NR_133657.1:n.437-287C>A (IGF2-AS)
NR_003512.4:n.708+1497G>T (INS-IGF2)
NM_001007139.6:c.-7+1497G>T (IGF2) NP_001007140.2:n.-7+1497G>T