Canonical Allele Identifier: CA344727859
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441253G>A , CM000663.2:g.218441253G>A GRCh38
NC_000001.10:g.218614595G>A , CM000663.1:g.218614595G>A GRCh37
NC_000001.9:g.216681218G>A NCBI36
NG_027721.1:g.100920G>A
NG_027721.2:g.100920G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.1136G>A MANE Select ENSP00000355897.4:p.Cys379Tyr
ENST00000366929.4:c.1220G>A ENSP00000355896.4:p.Cys407Tyr
ENST00000366930.8:c.1136G>A ENSP00000355897.4:p.Cys379Tyr
ENST00000479322.1:n.620G>A
NM_001135599.2:c.1220G>A NP_001129071.1:p.Cys407Tyr
NM_003238.3:c.1136G>A NP_003229.1:p.Cys379Tyr
NM_001135599.3:c.1220G>A NP_001129071.1:p.Cys407Tyr
NM_003238.4:c.1136G>A NP_003229.1:p.Cys379Tyr
NR_138148.1:n.2439G>A
NR_138149.1:n.2523G>A
NM_003238.5:c.1136G>A NP_003229.1:p.Cys379Tyr
NM_003238.6:c.1136G>A MANE Select NP_003229.1:p.Cys379Tyr
NM_001135599.4:c.1220G>A NP_001129071.1:p.Cys407Tyr
NR_138148.2:n.2387G>A
NR_138149.2:n.2471G>A