Canonical Allele Identifier: CA344727594
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437434A>C , CM000663.2:g.218437434A>C GRCh38
NC_000001.10:g.218610776A>C , CM000663.1:g.218610776A>C GRCh37
NC_000001.9:g.216677399A>C NCBI36
NG_027721.1:g.97101A>C
NG_027721.2:g.97101A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.1024A>C MANE Select ENSP00000355897.4:p.Asn342His
ENST00000366929.4:c.1108A>C ENSP00000355896.4:p.Asn370His
ENST00000366930.8:c.1024A>C ENSP00000355897.4:p.Asn342His
ENST00000479322.1:n.508A>C
NM_001135599.2:c.1108A>C NP_001129071.1:p.Asn370His
NM_003238.3:c.1024A>C NP_003229.1:p.Asn342His
NM_001135599.3:c.1108A>C NP_001129071.1:p.Asn370His
NM_003238.4:c.1024A>C NP_003229.1:p.Asn342His
NR_138148.1:n.2327A>C
NR_138149.1:n.2411A>C
NM_003238.5:c.1024A>C NP_003229.1:p.Asn342His
NM_003238.6:c.1024A>C MANE Select NP_003229.1:p.Asn342His
NM_001135599.4:c.1108A>C NP_001129071.1:p.Asn370His
NR_138148.2:n.2275A>C
NR_138149.2:n.2359A>C