Canonical Allele Identifier: CA127301046

Gene: AFF4

Linked Data

• dbSNP Id: rs932890959
• gnomAD v3: 5-132886211-G-A
• gnomAD v4: 5-132886211-G-A
• MyVariant Identifiers: chr5:g.132221903G>A (hg19) ; chr5:g.132886211G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886211G>A , CM000667.2:g.132886211G>A	GRCh38
NC_000005.9:g.132221903G>A , CM000667.1:g.132221903G>A	GRCh37
NC_000005.8:g.132249802G>A	NCBI36
NG_030340.1:g.82452C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265343.10:c.3099+99C>T MANE Select	ENSP00000265343.5:n.3099+99C>T
ENST00000265343.9:c.3099+99C>T	ENSP00000265343.5:n.3099+99C>T
NM_014423.3:c.3099+99C>T	NP_055238.1:n.3099+99C>T
XM_005271963.3:c.3099+99C>T	XP_005272020.1:n.3099+99C>T
XM_005271964.3:c.1965+99C>T	XP_005272021.1:n.1965+99C>T
XM_006714587.2:c.3012+99C>T	XP_006714650.1:n.3012+99C>T
XM_005271963.5:c.3099+99C>T	XP_005272020.1:n.3099+99C>T
XM_005271964.4:c.1965+99C>T	XP_005272021.1:n.1965+99C>T
XM_006714587.4:c.3012+99C>T	XP_006714650.1:n.3012+99C>T
NM_014423.4:c.3099+99C>T MANE Select	NP_055238.1:n.3099+99C>T