Canonical Allele Identifier: CA1583368756
Gene: AFF4 HGNC NCBI

Linked Data

dbSNP Id: rs1760115209

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886216G>C , CM000667.2:g.132886216G>C GRCh38
NC_000005.9:g.132221908G>C , CM000667.1:g.132221908G>C GRCh37
NC_000005.8:g.132249807G>C NCBI36
NG_030340.1:g.82447C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.3099+94C>G MANE Select ENSP00000265343.5:n.3099+94C>G
ENST00000265343.9:c.3099+94C>G ENSP00000265343.5:n.3099+94C>G
NM_014423.3:c.3099+94C>G NP_055238.1:n.3099+94C>G
XM_005271963.3:c.3099+94C>G XP_005272020.1:n.3099+94C>G
XM_005271964.3:c.1965+94C>G XP_005272021.1:n.1965+94C>G
XM_006714587.2:c.3012+94C>G XP_006714650.1:n.3012+94C>G
XM_005271963.5:c.3099+94C>G XP_005272020.1:n.3099+94C>G
XM_005271964.4:c.1965+94C>G XP_005272021.1:n.1965+94C>G
XM_006714587.4:c.3012+94C>G XP_006714650.1:n.3012+94C>G
NM_014423.4:c.3099+94C>G MANE Select NP_055238.1:n.3099+94C>G