Canonical Allele Identifier: CA151124313
Gene: IGF2R HGNC NCBI

Linked Data

dbSNP Id: rs998289535
MyVariant Identifiers: chr6:g.160430730T>C (hg19) chr6:g.160009698T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160009698T>C , CM000668.2:g.160009698T>C GRCh38
NC_000006.11:g.160430730T>C , CM000668.1:g.160430730T>C GRCh37
NC_000006.10:g.160350720T>C NCBI36
NG_011785.3:g.45600T>C
NG_011785.4:g.45600T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356956.6:c.414+564T>C MANE Select ENSP00000349437.1:n.414+564T>C
ENST00000676781.1:c.414+564T>C ENSP00000504419.1:n.414+564T>C
ENST00000677704.1:c.414+564T>C ENSP00000503314.1:n.414+564T>C
ENST00000356956.5:c.414+564T>C ENSP00000349437.1:n.414+564T>C
NM_000876.2:c.414+564T>C NP_000867.2:n.414+564T>C
XR_942419.1:n.429+564T>C
NM_000876.3:c.414+564T>C NP_000867.2:n.414+564T>C
NM_000876.4:c.414+564T>C MANE Select NP_000867.3:n.414+564T>C
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