Canonical Allele Identifier: CA1583368691
Gene: AFF4 HGNC NCBI

Linked Data

dbSNP Id: rs1760112876

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886115T>C , CM000667.2:g.132886115T>C GRCh38
NC_000005.9:g.132221807T>C , CM000667.1:g.132221807T>C GRCh37
NC_000005.8:g.132249706T>C NCBI36
NG_030340.1:g.82548A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3099+195A>G MANE Select ENSP00000265343.5:n.3099+195A>G
ENST00000265343.9:c.3099+195A>G ENSP00000265343.5:n.3099+195A>G
NM_014423.3:c.3099+195A>G NP_055238.1:n.3099+195A>G
XM_005271963.3:c.3099+195A>G XP_005272020.1:n.3099+195A>G
XM_005271964.3:c.1965+195A>G XP_005272021.1:n.1965+195A>G
XM_006714587.2:c.3012+195A>G XP_006714650.1:n.3012+195A>G
XM_005271963.5:c.3099+195A>G XP_005272020.1:n.3099+195A>G
XM_005271964.4:c.1965+195A>G XP_005272021.1:n.1965+195A>G
XM_006714587.4:c.3012+195A>G XP_006714650.1:n.3012+195A>G
NM_014423.4:c.3099+195A>G MANE Select NP_055238.1:n.3099+195A>G