Canonical Allele Identifier: CA1012386532
Gene: TGFB2 HGNC NCBI

Linked Data

dbSNP Id: rs1659999274

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437263T>C , CM000663.2:g.218437263T>C GRCh38
NC_000001.10:g.218610605T>C , CM000663.1:g.218610605T>C GRCh37
NC_000001.9:g.216677228T>C NCBI36
NG_027721.1:g.96930T>C
NG_027721.2:g.96930T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366930.9:c.933-80T>C MANE Select ENSP00000355897.4:n.933-80T>C
ENST00000366929.4:c.1017-80T>C ENSP00000355896.4:n.1017-80T>C
ENST00000366930.8:c.933-80T>C ENSP00000355897.4:n.933-80T>C
ENST00000479322.1:n.417-80T>C
NM_001135599.2:c.1017-80T>C NP_001129071.1:n.1017-80T>C
NM_003238.3:c.933-80T>C NP_003229.1:n.933-80T>C
NM_001135599.3:c.1017-80T>C NP_001129071.1:n.1017-80T>C
NM_003238.4:c.933-80T>C NP_003229.1:n.933-80T>C
NR_138148.1:n.2236-80T>C
NR_138149.1:n.2320-80T>C
NM_003238.5:c.933-80T>C NP_003229.1:n.933-80T>C
NM_003238.6:c.933-80T>C MANE Select NP_003229.1:n.933-80T>C
NM_001135599.4:c.1017-80T>C NP_001129071.1:n.1017-80T>C
NR_138148.2:n.2184-80T>C
NR_138149.2:n.2268-80T>C