Canonical Allele Identifier: CA2650508225
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345693A>G , CM000663.2:g.218345693A>G GRCh38
NC_000001.10:g.218519035A>G , CM000663.1:g.218519035A>G GRCh37
NC_000001.9:g.216585658A>G NCBI36
NG_027721.1:g.5360A>G
NG_027721.2:g.5360A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1009A>G MANE Select ENSP00000355897.4:n.-1009A>G
NM_001135599.2:c.-1009A>G NP_001129071.1:n.-1009A>G
NM_003238.3:c.-1009A>G NP_003229.1:n.-1009A>G
NM_001135599.3:c.-1009A>G NP_001129071.1:n.-1009A>G
NM_003238.4:c.-1009A>G NP_003229.1:n.-1009A>G
NR_138148.1:n.410A>G
NR_138149.1:n.410A>G
NM_003238.5:c.-1009A>G NP_003229.1:n.-1009A>G
NM_003238.6:c.-1009A>G MANE Select NP_003229.1:n.-1009A>G
NM_001135599.4:c.-1009A>G NP_001129071.1:n.-1009A>G
NR_138148.2:n.358A>G
NR_138149.2:n.358A>G