Canonical Allele Identifier: CA850261459

Gene: EBF2

Linked Data

• dbSNP Id: rs1448954617
• MyVariant Identifiers: chr8:g.25891971G>A (hg19) ; chr8:g.26034455G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26034455G>A , CM000670.2:g.26034455G>A	GRCh38
NC_000008.10:g.25891971G>A , CM000670.1:g.25891971G>A	GRCh37
NC_000008.9:g.25947888G>A	NCBI36
NG_030344.1:g.15670C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000520164.6:c.483-1302C>T MANE Select	ENSP00000430241.1:n.483-1302C>T
ENST00000408929.7:c.39-1302C>T	ENSP00000386178.3:n.39-1302C>T
ENST00000517825.1:n.802-1302C>T
ENST00000520164.5:c.483-1302C>T	ENSP00000430241.1:n.483-1302C>T
NM_022659.3:c.483-1302C>T	NP_073150.2:n.483-1302C>T
NM_022659.4:c.483-1302C>T MANE Select	NP_073150.2:n.483-1302C>T