Canonical Allele Identifier: CA174555418

Gene: EBF2

Linked Data

• dbSNP Id: rs966911366
• MyVariant Identifiers: chr8:g.25892073A>G (hg19) ; chr8:g.26034557A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26034557A>G , CM000670.2:g.26034557A>G	GRCh38
NC_000008.10:g.25892073A>G , CM000670.1:g.25892073A>G	GRCh37
NC_000008.9:g.25947990A>G	NCBI36
NG_030344.1:g.15568T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000520164.6:c.483-1404T>C MANE Select	ENSP00000430241.1:n.483-1404T>C
ENST00000408929.7:c.39-1404T>C	ENSP00000386178.3:n.39-1404T>C
ENST00000517825.1:n.802-1404T>C
ENST00000520164.5:c.483-1404T>C	ENSP00000430241.1:n.483-1404T>C
NM_022659.3:c.483-1404T>C	NP_073150.2:n.483-1404T>C
NM_022659.4:c.483-1404T>C MANE Select	NP_073150.2:n.483-1404T>C