Canonical Allele Identifier: CA199681
Gene: AFF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 190331
ClinVar RCV Id: RCV000170517 RCV000485909
dbSNP Id: rs786205680
MyVariant Identifiers: chr5:g.132269985G>A (hg19) chr5:g.132934293G>A (hg38)
PubMed: PMID:25730767
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934293G>A , CM000667.2:g.132934293G>A GRCh38
NC_000005.9:g.132269985G>A , CM000667.1:g.132269985G>A GRCh37
NC_000005.8:g.132297884G>A NCBI36
NG_030340.1:g.34370C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.772C>T MANE Select ENSP00000265343.5:p.Arg258Trp
ENST00000265343.9:c.772C>T ENSP00000265343.5:p.Arg258Trp
ENST00000378595.7:c.772C>T ENSP00000367858.3:p.Arg258Trp
ENST00000465484.1:n.1031C>T
ENST00000491831.5:n.1032C>T
NM_014423.3:c.772C>T NP_055238.1:p.Arg258Trp
XM_005271963.3:c.772C>T XP_005272020.1:p.Arg258Trp
XM_006714587.2:c.772C>T XP_006714650.1:p.Arg258Trp
XM_005271963.5:c.772C>T XP_005272020.1:p.Arg258Trp
XM_006714587.4:c.772C>T XP_006714650.1:p.Arg258Trp
NM_014423.4:c.772C>T MANE Select NP_055238.1:p.Arg258Trp
Search 100 bp 5'
Search 100 bp 3'