Canonical Allele Identifier: CA1221527965
Gene: TGFB2 HGNC NCBI
TGFB2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1656628584

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345464T>C , CM000663.2:g.218345464T>C GRCh38
NC_000001.10:g.218518806T>C , CM000663.1:g.218518806T>C GRCh37
NC_000001.9:g.216585429T>C NCBI36
NG_027721.1:g.5131T>C
NG_027721.2:g.5131T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1238T>C (TGFB2) MANE Select ENSP00000355897.4:n.-1238T>C
NM_001135599.2:c.-1238T>C (TGFB2) NP_001129071.1:n.-1238T>C
NM_003238.3:c.-1238T>C (TGFB2) NP_003229.1:n.-1238T>C
NR_046268.1:n.77-76A>G (TGFB2-AS1)
NM_001135599.3:c.-1238T>C (TGFB2) NP_001129071.1:n.-1238T>C
NM_003238.4:c.-1238T>C (TGFB2) NP_003229.1:n.-1238T>C
NR_138148.1:n.181T>C (TGFB2)
NR_138149.1:n.181T>C (TGFB2)
NM_003238.5:c.-1238T>C (TGFB2) NP_003229.1:n.-1238T>C
NM_003238.6:c.-1238T>C (TGFB2) MANE Select NP_003229.1:n.-1238T>C
NM_001135599.4:c.-1238T>C (TGFB2) NP_001129071.1:n.-1238T>C
NR_138148.2:n.129T>C (TGFB2)
NR_138149.2:n.129T>C (TGFB2)