Canonical Allele Identifier: CA344725410
Gene: TGFB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405235
ClinVar RCV Id: RCV001903650
dbSNP Id: rs1431335293

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346857T>G , CM000663.2:g.218346857T>G GRCh38
NC_000001.10:g.218520199T>G , CM000663.1:g.218520199T>G GRCh37
NC_000001.9:g.216586822T>G NCBI36
NG_027721.1:g.6524T>G
NG_027721.2:g.6524T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.156T>G MANE Select ENSP00000355897.4:p.Ser52Arg
ENST00000366929.4:c.156T>G ENSP00000355896.4:p.Ser52Arg
ENST00000366930.8:c.156T>G ENSP00000355897.4:p.Ser52Arg
NM_001135599.2:c.156T>G NP_001129071.1:p.Ser52Arg
NM_003238.3:c.156T>G NP_003229.1:p.Ser52Arg
NM_001135599.3:c.156T>G NP_001129071.1:p.Ser52Arg
NM_003238.4:c.156T>G NP_003229.1:p.Ser52Arg
NR_138148.1:n.1574T>G
NR_138149.1:n.1574T>G
NM_003238.5:c.156T>G NP_003229.1:p.Ser52Arg
NM_003238.6:c.156T>G MANE Select NP_003229.1:p.Ser52Arg
NM_001135599.4:c.156T>G NP_001129071.1:p.Ser52Arg
NR_138148.2:n.1522T>G
NR_138149.2:n.1522T>G