Canonical Allele Identifier: CA3408751

Gene: AFF4

Linked Data

• dbSNP Id: rs149046818
• ExAC: 5:132222014 T / G
• gnomAD v2: 5-132222014-T-G
• gnomAD v3: 5-132886322-T-G
• gnomAD v4: 5-132886322-T-G
• MyVariant Identifiers: chr5:g.132222014T>G (hg19) ; chr5:g.132886322T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886322T>G , CM000667.2:g.132886322T>G	GRCh38
NC_000005.9:g.132222014T>G , CM000667.1:g.132222014T>G	GRCh37
NC_000005.8:g.132249913T>G	NCBI36
NG_030340.1:g.82341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.3087A>C MANE Select	ENSP00000265343.5:p.Thr1029=
ENST00000265343.9:c.3087A>C	ENSP00000265343.5:p.Thr1029=
NM_014423.3:c.3087A>C	NP_055238.1:p.Thr1029=
XM_005271963.3:c.3087A>C	XP_005272020.1:p.Thr1029=
XM_005271964.3:c.1953A>C	XP_005272021.1:p.Thr651=
XM_006714587.2:c.3000A>C	XP_006714650.1:p.Thr1000=
XM_005271963.5:c.3087A>C	XP_005272020.1:p.Thr1029=
XM_005271964.4:c.1953A>C	XP_005272021.1:p.Thr651=
XM_006714587.4:c.3000A>C	XP_006714650.1:p.Thr1000=
NM_014423.4:c.3087A>C MANE Select	NP_055238.1:p.Thr1029=