Canonical Allele Identifier: CA821586746
Gene: IGF2R HGNC NCBI

Linked Data

dbSNP Id: rs1318044784
MyVariant Identifiers: chr6:g.160430652A>C (hg19) chr6:g.160009620A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160009620A>C , CM000668.2:g.160009620A>C GRCh38
NC_000006.11:g.160430652A>C , CM000668.1:g.160430652A>C GRCh37
NC_000006.10:g.160350642A>C NCBI36
NG_011785.3:g.45522A>C
NG_011785.4:g.45522A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356956.6:c.414+486A>C MANE Select ENSP00000349437.1:n.414+486A>C
ENST00000676781.1:c.414+486A>C ENSP00000504419.1:n.414+486A>C
ENST00000677704.1:c.414+486A>C ENSP00000503314.1:n.414+486A>C
ENST00000356956.5:c.414+486A>C ENSP00000349437.1:n.414+486A>C
NM_000876.2:c.414+486A>C NP_000867.2:n.414+486A>C
XR_942419.1:n.429+486A>C
NM_000876.3:c.414+486A>C NP_000867.2:n.414+486A>C
NM_000876.4:c.414+486A>C MANE Select NP_000867.3:n.414+486A>C
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