Canonical Allele Identifier: CA1772168920
Gene: EBF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034472C= , CM000670.2:g.26034472C= GRCh38
NC_000008.10:g.25891988C= , CM000670.1:g.25891988C= GRCh37
NC_000008.9:g.25947905C= NCBI36
NG_030344.1:g.15653G=

Transcript Alleles

HGVS Amino-acid change
ENST00000520164.6:c.483-1319G= MANE Select ENSP00000430241.1:n.483-1319G=
ENST00000408929.7:c.39-1319G= ENSP00000386178.3:n.39-1319G=
ENST00000517825.1:n.802-1319G=
ENST00000520164.5:c.483-1319G= ENSP00000430241.1:n.483-1319G=
NM_022659.3:c.483-1319G= NP_073150.2:n.483-1319G=
NM_022659.4:c.483-1319G= MANE Select NP_073150.2:n.483-1319G=