Canonical Allele Identifier: CA446498907
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132228006G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892314G>T , CM000667.2:g.132892314G>T GRCh38
NC_000005.9:g.132228006G>T , CM000667.1:g.132228006G>T GRCh37
NC_000005.8:g.132255905G>T NCBI36
NG_030340.1:g.76349C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.2487C>A MANE Select ENSP00000265343.5:p.Gly829=
ENST00000265343.9:c.2487C>A ENSP00000265343.5:p.Gly829=
ENST00000378595.7:c.2487C>A ENSP00000367858.3:p.Gly829=
NM_014423.3:c.2487C>A NP_055238.1:p.Gly829=
XM_005271963.3:c.2487C>A XP_005272020.1:p.Gly829=
XM_005271964.3:c.1353C>A XP_005272021.1:p.Gly451=
XM_006714587.2:c.2400C>A XP_006714650.1:p.Gly800=
XM_005271963.5:c.2487C>A XP_005272020.1:p.Gly829=
XM_005271964.4:c.1353C>A XP_005272021.1:p.Gly451=
XM_006714587.4:c.2400C>A XP_006714650.1:p.Gly800=
NM_014423.4:c.2487C>A MANE Select NP_055238.1:p.Gly829=