Canonical Allele Identifier: CA1772169056
Gene: EBF2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034590G= , CM000670.2:g.26034590G= GRCh38
NC_000008.10:g.25892106G= , CM000670.1:g.25892106G= GRCh37
NC_000008.9:g.25948023G= NCBI36
NG_030344.1:g.15535C=

Transcript Alleles

HGVS Amino-acid change
ENST00000520164.6:c.483-1437C= MANE Select ENSP00000430241.1:n.483-1437C=
ENST00000408929.7:c.39-1437C= ENSP00000386178.3:n.39-1437C=
ENST00000517825.1:n.802-1437C=
ENST00000520164.5:c.483-1437C= ENSP00000430241.1:n.483-1437C=
NM_022659.3:c.483-1437C= NP_073150.2:n.483-1437C=
NM_022659.4:c.483-1437C= MANE Select NP_073150.2:n.483-1437C=
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