Canonical Allele Identifier: CA2570166964
Gene: EBF2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034598A>C , CM000670.2:g.26034598A>C GRCh38
NC_000008.10:g.25892114A>C , CM000670.1:g.25892114A>C GRCh37
NC_000008.9:g.25948031A>C NCBI36
NG_030344.1:g.15527T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000520164.6:c.483-1445T>G MANE Select ENSP00000430241.1:n.483-1445T>G
ENST00000408929.7:c.39-1445T>G ENSP00000386178.3:n.39-1445T>G
ENST00000517825.1:n.802-1445T>G
ENST00000520164.5:c.483-1445T>G ENSP00000430241.1:n.483-1445T>G
NM_022659.3:c.483-1445T>G NP_073150.2:n.483-1445T>G
NM_022659.4:c.483-1445T>G MANE Select NP_073150.2:n.483-1445T>G
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