Canonical Allele Identifier: CA151124251
Gene: IGF2R HGNC NCBI

Linked Data

dbSNP Id: rs8191732
MyVariant Identifiers: chr6:g.160430631A>G (hg19) chr6:g.160009599A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160009599A>G , CM000668.2:g.160009599A>G GRCh38
NC_000006.11:g.160430631A>G , CM000668.1:g.160430631A>G GRCh37
NC_000006.10:g.160350621A>G NCBI36
NG_011785.3:g.45501A>G
NG_011785.4:g.45501A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356956.6:c.414+465A>G MANE Select ENSP00000349437.1:n.414+465A>G
ENST00000676781.1:c.414+465A>G ENSP00000504419.1:n.414+465A>G
ENST00000677704.1:c.414+465A>G ENSP00000503314.1:n.414+465A>G
ENST00000356956.5:c.414+465A>G ENSP00000349437.1:n.414+465A>G
NM_000876.2:c.414+465A>G NP_000867.2:n.414+465A>G
XR_942419.1:n.429+465A>G
NM_000876.3:c.414+465A>G NP_000867.2:n.414+465A>G
NM_000876.4:c.414+465A>G MANE Select NP_000867.3:n.414+465A>G
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