Canonical Allele Identifier: CA446498812
Gene: AFF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.132227874A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892182A>G , CM000667.2:g.132892182A>G GRCh38
NC_000005.9:g.132227874A>G , CM000667.1:g.132227874A>G GRCh37
NC_000005.8:g.132255773A>G NCBI36
NG_030340.1:g.76481T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2619T>C MANE Select ENSP00000265343.5:p.Ser873=
ENST00000265343.9:c.2619T>C ENSP00000265343.5:p.Ser873=
ENST00000378595.7:c.2619T>C ENSP00000367858.3:p.Ser873=
NM_014423.3:c.2619T>C NP_055238.1:p.Ser873=
XM_005271963.3:c.2619T>C XP_005272020.1:p.Ser873=
XM_005271964.3:c.1485T>C XP_005272021.1:p.Ser495=
XM_006714587.2:c.2532T>C XP_006714650.1:p.Ser844=
XM_005271963.5:c.2619T>C XP_005272020.1:p.Ser873=
XM_005271964.4:c.1485T>C XP_005272021.1:p.Ser495=
XM_006714587.4:c.2532T>C XP_006714650.1:p.Ser844=
NM_014423.4:c.2619T>C MANE Select NP_055238.1:p.Ser873=