Canonical Allele Identifier: CA2574134784
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441386C>T , CM000663.2:g.218441386C>T GRCh38
NC_000001.10:g.218614728C>T , CM000663.1:g.218614728C>T GRCh37
NC_000001.9:g.216681351C>T NCBI36
NG_027721.1:g.101053C>T
NG_027721.2:g.101053C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.*24C>T MANE Select ENSP00000355897.4:n.*24C>T
ENST00000366929.4:c.*24C>T ENSP00000355896.4:n.*24C>T
ENST00000366930.8:c.*24C>T ENSP00000355897.4:n.*24C>T
ENST00000479322.1:n.753C>T
NM_001135599.2:c.*24C>T NP_001129071.1:n.*24C>T
NM_003238.3:c.*24C>T NP_003229.1:n.*24C>T
NM_001135599.3:c.*24C>T NP_001129071.1:n.*24C>T
NM_003238.4:c.*24C>T NP_003229.1:n.*24C>T
NR_138148.1:n.2572C>T
NR_138149.1:n.2656C>T
NM_003238.5:c.*24C>T NP_003229.1:n.*24C>T
NM_003238.6:c.*24C>T MANE Select NP_003229.1:n.*24C>T
NM_001135599.4:c.*24C>T NP_001129071.1:n.*24C>T
NR_138148.2:n.2520C>T
NR_138149.2:n.2604C>T