Canonical Allele Identifier: CA446498827
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132227886C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892194C>A , CM000667.2:g.132892194C>A GRCh38
NC_000005.9:g.132227886C>A , CM000667.1:g.132227886C>A GRCh37
NC_000005.8:g.132255785C>A NCBI36
NG_030340.1:g.76469G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2607G>T MANE Select ENSP00000265343.5:p.Gly869=
ENST00000265343.9:c.2607G>T ENSP00000265343.5:p.Gly869=
ENST00000378595.7:c.2607G>T ENSP00000367858.3:p.Gly869=
NM_014423.3:c.2607G>T NP_055238.1:p.Gly869=
XM_005271963.3:c.2607G>T XP_005272020.1:p.Gly869=
XM_005271964.3:c.1473G>T XP_005272021.1:p.Gly491=
XM_006714587.2:c.2520G>T XP_006714650.1:p.Gly840=
XM_005271963.5:c.2607G>T XP_005272020.1:p.Gly869=
XM_005271964.4:c.1473G>T XP_005272021.1:p.Gly491=
XM_006714587.4:c.2520G>T XP_006714650.1:p.Gly840=
NM_014423.4:c.2607G>T MANE Select NP_055238.1:p.Gly869=