Canonical Allele Identifier: CA174555404
Gene: EBF2 HGNC NCBI

Linked Data

dbSNP Id: rs538086602
gnomAD v2: 8-25891972-G-C
gnomAD v3: 8-26034456-G-C
gnomAD v4: 8-26034456-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034456G>C , CM000670.2:g.26034456G>C GRCh38
NC_000008.10:g.25891972G>C , CM000670.1:g.25891972G>C GRCh37
NC_000008.9:g.25947889G>C NCBI36
NG_030344.1:g.15669C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000520164.6:c.483-1303C>G MANE Select ENSP00000430241.1:n.483-1303C>G
ENST00000408929.7:c.39-1303C>G ENSP00000386178.3:n.39-1303C>G
ENST00000517825.1:n.802-1303C>G
ENST00000520164.5:c.483-1303C>G ENSP00000430241.1:n.483-1303C>G
NM_022659.3:c.483-1303C>G NP_073150.2:n.483-1303C>G
NM_022659.4:c.483-1303C>G MANE Select NP_073150.2:n.483-1303C>G