Canonical Allele Identifier: CA850261489
Gene: EBF2 HGNC NCBI

Linked Data

dbSNP Id: rs1165526717
MyVariant Identifiers: chr8:g.25892030C>T (hg19) chr8:g.26034514C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034514C>T , CM000670.2:g.26034514C>T GRCh38
NC_000008.10:g.25892030C>T , CM000670.1:g.25892030C>T GRCh37
NC_000008.9:g.25947947C>T NCBI36
NG_030344.1:g.15611G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000520164.6:c.483-1361G>A MANE Select ENSP00000430241.1:n.483-1361G>A
ENST00000408929.7:c.39-1361G>A ENSP00000386178.3:n.39-1361G>A
ENST00000517825.1:n.802-1361G>A
ENST00000520164.5:c.483-1361G>A ENSP00000430241.1:n.483-1361G>A
NM_022659.3:c.483-1361G>A NP_073150.2:n.483-1361G>A
NM_022659.4:c.483-1361G>A MANE Select NP_073150.2:n.483-1361G>A
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