Canonical Allele Identifier: CA804039637

Gene: AFF4

Linked Data

• dbSNP Id: rs1383961987
• gnomAD v3: 5-132886214-G-A
• gnomAD v4: 5-132886214-G-A
• MyVariant Identifiers: chr5:g.132221906G>A (hg19) ; chr5:g.132886214G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132886214G>A , CM000667.2:g.132886214G>A	GRCh38
NC_000005.9:g.132221906G>A , CM000667.1:g.132221906G>A	GRCh37
NC_000005.8:g.132249805G>A	NCBI36
NG_030340.1:g.82449C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.3099+96C>T MANE Select	ENSP00000265343.5:n.3099+96C>T
ENST00000265343.9:c.3099+96C>T	ENSP00000265343.5:n.3099+96C>T
NM_014423.3:c.3099+96C>T	NP_055238.1:n.3099+96C>T
XM_005271963.3:c.3099+96C>T	XP_005272020.1:n.3099+96C>T
XM_005271964.3:c.1965+96C>T	XP_005272021.1:n.1965+96C>T
XM_006714587.2:c.3012+96C>T	XP_006714650.1:n.3012+96C>T
XM_005271963.5:c.3099+96C>T	XP_005272020.1:n.3099+96C>T
XM_005271964.4:c.1965+96C>T	XP_005272021.1:n.1965+96C>T
XM_006714587.4:c.3012+96C>T	XP_006714650.1:n.3012+96C>T
NM_014423.4:c.3099+96C>T MANE Select	NP_055238.1:n.3099+96C>T