Canonical Allele Identifier: CA360957403
Gene: AFF4 HGNC NCBI

Linked Data

dbSNP Id: rs1761365432

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934197T>C , CM000667.2:g.132934197T>C GRCh38
NC_000005.9:g.132269889T>C , CM000667.1:g.132269889T>C GRCh37
NC_000005.8:g.132297788T>C NCBI36
NG_030340.1:g.34466A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.868A>G MANE Select ENSP00000265343.5:p.Ser290Gly
ENST00000265343.9:c.868A>G ENSP00000265343.5:p.Ser290Gly
ENST00000378593.6:n.35A>G
ENST00000378595.7:c.868A>G ENSP00000367858.3:p.Ser290Gly
ENST00000425658.1:c.42A>G
ENST00000465484.1:n.1127A>G
ENST00000491831.5:n.1128A>G
NM_014423.3:c.868A>G NP_055238.1:p.Ser290Gly
XM_005271963.3:c.868A>G XP_005272020.1:p.Ser290Gly
XM_006714587.2:c.868A>G XP_006714650.1:p.Ser290Gly
XM_005271963.5:c.868A>G XP_005272020.1:p.Ser290Gly
XM_006714587.4:c.868A>G XP_006714650.1:p.Ser290Gly
NM_014423.4:c.868A>G MANE Select NP_055238.1:p.Ser290Gly