Canonical Allele Identifier: CA452889496
Gene: IGF2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160453999A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160032967A>G , CM000668.2:g.160032967A>G GRCh38
NC_000006.11:g.160453999A>G , CM000668.1:g.160453999A>G GRCh37
NC_000006.10:g.160373989A>G NCBI36
NG_011785.3:g.68869A>G
NG_011785.4:g.68869A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356956.6:c.1071A>G MANE Select ENSP00000349437.1:p.Lys357=
ENST00000649737.1:n.308A>G
ENST00000676781.1:c.1071A>G ENSP00000504419.1:p.Lys357=
ENST00000677704.1:c.1071A>G ENSP00000503314.1:p.Lys357=
ENST00000356956.5:c.1071A>G ENSP00000349437.1:p.Lys357=
NM_000876.2:c.1071A>G NP_000867.2:p.Lys357=
XR_942419.1:n.1086A>G
NM_000876.3:c.1071A>G NP_000867.2:p.Lys357=
NM_000876.4:c.1071A>G MANE Select NP_000867.3:p.Lys357=
Search 100 bp 5'
Search 100 bp 3'