Canonical Allele Identifier: CA850261463
Gene: EBF2 HGNC NCBI

Linked Data

dbSNP Id: rs1204270168
gnomAD v3: 8-26034470-A-G
gnomAD v4: 8-26034470-A-G
MyVariant Identifiers: chr8:g.25891986A>G (hg19) chr8:g.26034470A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034470A>G , CM000670.2:g.26034470A>G GRCh38
NC_000008.10:g.25891986A>G , CM000670.1:g.25891986A>G GRCh37
NC_000008.9:g.25947903A>G NCBI36
NG_030344.1:g.15655T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000520164.6:c.483-1317T>C MANE Select ENSP00000430241.1:n.483-1317T>C
ENST00000408929.7:c.39-1317T>C ENSP00000386178.3:n.39-1317T>C
ENST00000517825.1:n.802-1317T>C
ENST00000520164.5:c.483-1317T>C ENSP00000430241.1:n.483-1317T>C
NM_022659.3:c.483-1317T>C NP_073150.2:n.483-1317T>C
NM_022659.4:c.483-1317T>C MANE Select NP_073150.2:n.483-1317T>C
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