Canonical Allele Identifier: CA1676853812
Gene: IGF2R HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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