Canonical Allele Identifier: CA452889495
Gene: IGF2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.160453996A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160032964A>C , CM000668.2:g.160032964A>C GRCh38
NC_000006.11:g.160453996A>C , CM000668.1:g.160453996A>C GRCh37
NC_000006.10:g.160373986A>C NCBI36
NG_011785.3:g.68866A>C
NG_011785.4:g.68866A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356956.6:c.1068A>C MANE Select ENSP00000349437.1:p.Gly356=
ENST00000649737.1:n.305A>C
ENST00000676781.1:c.1068A>C ENSP00000504419.1:p.Gly356=
ENST00000677704.1:c.1068A>C ENSP00000503314.1:p.Gly356=
ENST00000356956.5:c.1068A>C ENSP00000349437.1:p.Gly356=
NM_000876.2:c.1068A>C NP_000867.2:p.Gly356=
XR_942419.1:n.1083A>C
NM_000876.3:c.1068A>C NP_000867.2:p.Gly356=
NM_000876.4:c.1068A>C MANE Select NP_000867.3:p.Gly356=
Search 100 bp 5'
Search 100 bp 3'