Canonical Allele Identifier: CA216260498

Gene: IGF2 INS-IGF2 IGF2-AS

Linked Data

• dbSNP Id: rs553662656
• gnomAD v4: 11-2146370-G-T
• MyVariant Identifiers: chr11:g.2167600G>T (hg19) ; chr11:g.2146370G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2146370G>T , CM000673.2:g.2146370G>T	GRCh38
NC_000011.9:g.2167600G>T , CM000673.1:g.2167600G>T	GRCh37
NC_000011.8:g.2124176G>T	NCBI36
NG_008849.1:g.8234C>A
NG_050578.1:g.19840C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-7+1196C>A (IGF2)	ENSP00000511998.1:n.-7+1196C>A
ENST00000643349.2:c.*46+1196C>A	ENSP00000495715.1:n.*46+1196C>A
ENST00000695541.1:c.-7+1196C>A (IGF2)	ENSP00000511997.1:n.-7+1196C>A
ENST00000643349.1:c.*46+1196C>A	ENSP00000495715.1:n.*46+1196C>A
ENST00000356578.8:c.*46+1196C>A (INS-IGF2)	ENSP00000348986.4:n.*46+1196C>A
NM_001007139.5:c.-7+1196C>A (IGF2)	NP_001007140.2:n.-7+1196C>A
NR_003512.3:n.708+1196C>A (INS-IGF2)
NR_028043.2:n.562G>T (IGF2-AS)
NR_133657.1:n.451G>T (IGF2-AS)
NR_003512.4:n.708+1196C>A (INS-IGF2)
NM_001007139.6:c.-7+1196C>A (IGF2)	NP_001007140.2:n.-7+1196C>A