Canonical Allele Identifier: CA2528032423
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133757136G>T , CM000665.2:g.133757136G>T GRCh38
NC_000003.11:g.133475980G>T , CM000665.1:g.133475980G>T GRCh37
NC_000003.10:g.134958670G>T NCBI36
NG_013080.1:g.16004G>T
NG_013080.2:g.100139G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.870+127G>T MANE Select ENSP00000385834.3:n.870+127G>T
ENST00000402696.7:c.870+127G>T ENSP00000385834.3:n.870+127G>T
ENST00000485977.1:c.235+127G>T ENSP00000418716.1:n.235+127G>T
NM_001063.3:c.870+127G>T NP_001054.1:n.870+127G>T
XM_011513100.1:c.870+127G>T XP_011511402.1:n.870+127G>T
NM_001354703.1:c.738+127G>T NP_001341632.1:n.738+127G>T
NM_001354704.1:c.489+127G>T NP_001341633.1:n.489+127G>T
NM_001063.4:c.870+127G>T MANE Select NP_001054.2:n.870+127G>T
NM_001354703.2:c.738+127G>T NP_001341632.2:n.738+127G>T
NM_001354704.2:c.489+127G>T NP_001341633.2:n.489+127G>T