Canonical Allele Identifier: CA344725398
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346850T>G , CM000663.2:g.218346850T>G GRCh38
NC_000001.10:g.218520192T>G , CM000663.1:g.218520192T>G GRCh37
NC_000001.9:g.216586815T>G NCBI36
NG_027721.1:g.6517T>G
NG_027721.2:g.6517T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.149T>G MANE Select ENSP00000355897.4:p.Leu50Arg
ENST00000366929.4:c.149T>G ENSP00000355896.4:p.Leu50Arg
ENST00000366930.8:c.149T>G ENSP00000355897.4:p.Leu50Arg
NM_001135599.2:c.149T>G NP_001129071.1:p.Leu50Arg
NM_003238.3:c.149T>G NP_003229.1:p.Leu50Arg
NM_001135599.3:c.149T>G NP_001129071.1:p.Leu50Arg
NM_003238.4:c.149T>G NP_003229.1:p.Leu50Arg
NR_138148.1:n.1567T>G
NR_138149.1:n.1567T>G
NM_003238.5:c.149T>G NP_003229.1:p.Leu50Arg
NM_003238.6:c.149T>G MANE Select NP_003229.1:p.Leu50Arg
NM_001135599.4:c.149T>G NP_001129071.1:p.Leu50Arg
NR_138148.2:n.1515T>G
NR_138149.2:n.1515T>G