Canonical Allele Identifier: CA1221527998
Gene: TGFB2 HGNC NCBI
TGFB2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1048322487

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345521C>G , CM000663.2:g.218345521C>G GRCh38
NC_000001.10:g.218518863C>G , CM000663.1:g.218518863C>G GRCh37
NC_000001.9:g.216585486C>G NCBI36
NG_027721.1:g.5188C>G
NG_027721.2:g.5188C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1181C>G (TGFB2) MANE Select ENSP00000355897.4:n.-1181C>G
NM_001135599.2:c.-1181C>G (TGFB2) NP_001129071.1:n.-1181C>G
NM_003238.3:c.-1181C>G (TGFB2) NP_003229.1:n.-1181C>G
NR_046268.1:n.76+82G>C (TGFB2-AS1)
NM_001135599.3:c.-1181C>G (TGFB2) NP_001129071.1:n.-1181C>G
NM_003238.4:c.-1181C>G (TGFB2) NP_003229.1:n.-1181C>G
NR_138148.1:n.238C>G (TGFB2)
NR_138149.1:n.238C>G (TGFB2)
NM_003238.5:c.-1181C>G (TGFB2) NP_003229.1:n.-1181C>G
NM_003238.6:c.-1181C>G (TGFB2) MANE Select NP_003229.1:n.-1181C>G
NM_001135599.4:c.-1181C>G (TGFB2) NP_001129071.1:n.-1181C>G
NR_138148.2:n.186C>G (TGFB2)
NR_138149.2:n.186C>G (TGFB2)