Canonical Allele Identifier: CA674520790

Gene: INS-IGF2

Linked Data

• dbSNP Id: rs1432930780
• gnomAD v3: 11-2159733-T-TG
• gnomAD v4: 11-2159733-T-TG
• MyVariant Identifiers: chr11:g.2180963_2180964insG (hg19) ; chr11:g.2159733_2159734insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2159737dup , CM000673.2:g.2159737dup	GRCh38
NC_000011.9:g.2180967dup , CM000673.1:g.2180967dup	GRCh37
NC_000011.8:g.2137543dup	NCBI36
NG_007114.1:g.6461dup
NG_050578.1:g.6476dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356578.8:c.187+1051dup	ENSP00000348986.4:n.187+1051dup
ENST00000397270.1:c.187+1051dup	ENSP00000380440.1:n.187+1051dup
NM_001042376.2:c.187+1051dup	NP_001035835.1:n.187+1051dup
NR_003512.3:n.246+1051dup
NM_001042376.3:c.187+1051dup	NP_001035835.1:n.187+1051dup
NR_003512.4:n.246+1051dup