Canonical Allele Identifier: CA15491696
Gene: IGF2BP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23381148A>C , CM000669.2:g.23381148A>C GRCh38
NC_000007.13:g.23420767A>C , CM000669.1:g.23420767A>C GRCh37
NC_000007.12:g.23387292A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258729.8:c.286-19407T>G MANE Select ENSP00000258729.3:n.286-19407T>G
ENST00000258729.7:c.286-19407T>G ENSP00000258729.3:n.286-19407T>G
ENST00000421467.6:c.237-19551T>G ENSP00000395936.1:n.237-19551T>G
ENST00000465058.5:n.276-19407T>G
ENST00000466809.6:n.180-19407T>G
ENST00000468263.5:n.205-19407T>G
ENST00000469723.5:n.185-18473T>G
ENST00000474105.5:n.467-19407T>G
ENST00000476938.5:n.192-19407T>G
ENST00000479504.5:n.178-19551T>G
ENST00000491719.5:n.485-19407T>G
ENST00000492771.5:n.94+13436T>G
NM_006547.2:c.286-19407T>G NP_006538.2:n.286-19407T>G
XM_006715639.1:c.-186-19407T>G XP_006715702.1:n.-186-19407T>G
XM_011515089.1:c.301-19407T>G XP_011513391.1:n.301-19407T>G
XM_011515090.1:c.78-29562T>G XP_011513392.1:n.78-29562T>G
XM_011515091.1:c.-70-29562T>G XP_011513393.1:n.-70-29562T>G
XM_011515092.1:c.7-19407T>G XP_011513394.1:n.7-19407T>G
XM_011515093.1:c.7-19407T>G XP_011513395.1:n.7-19407T>G
XM_006715639.2:c.-186-19407T>G XP_006715702.1:n.-186-19407T>G
XM_011515089.2:c.301-19407T>G XP_011513391.1:n.301-19407T>G
XM_011515090.3:c.78-29562T>G XP_011513392.1:n.78-29562T>G
XM_011515091.2:c.-70-29562T>G XP_011513393.1:n.-70-29562T>G
XM_011515092.2:c.7-19407T>G XP_011513394.1:n.7-19407T>G
XM_011515093.2:c.7-19407T>G XP_011513395.1:n.7-19407T>G
NM_006547.3:c.286-19407T>G MANE Select NP_006538.2:n.286-19407T>G
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