Canonical Allele Identifier: CA2650508213

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218345681-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345681A>G , CM000663.2:g.218345681A>G	GRCh38
NC_000001.10:g.218519023A>G , CM000663.1:g.218519023A>G	GRCh37
NC_000001.9:g.216585646A>G	NCBI36
NG_027721.1:g.5348A>G
NG_027721.2:g.5348A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-1021A>G MANE Select	ENSP00000355897.4:n.-1021A>G
NM_001135599.2:c.-1021A>G	NP_001129071.1:n.-1021A>G
NM_003238.3:c.-1021A>G	NP_003229.1:n.-1021A>G
NM_001135599.3:c.-1021A>G	NP_001129071.1:n.-1021A>G
NM_003238.4:c.-1021A>G	NP_003229.1:n.-1021A>G
NR_138148.1:n.398A>G
NR_138149.1:n.398A>G
NM_003238.5:c.-1021A>G	NP_003229.1:n.-1021A>G
NM_003238.6:c.-1021A>G MANE Select	NP_003229.1:n.-1021A>G
NM_001135599.4:c.-1021A>G	NP_001129071.1:n.-1021A>G
NR_138148.2:n.346A>G
NR_138149.2:n.346A>G