Canonical Allele Identifier: CA2574134758

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218437521-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437521C>G , CM000663.2:g.218437521C>G	GRCh38
NC_000001.10:g.218610863C>G , CM000663.1:g.218610863C>G	GRCh37
NC_000001.9:g.216677486C>G	NCBI36
NG_027721.1:g.97188C>G
NG_027721.2:g.97188C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1086+25C>G MANE Select	ENSP00000355897.4:n.1086+25C>G
ENST00000366929.4:c.1170+25C>G	ENSP00000355896.4:n.1170+25C>G
ENST00000366930.8:c.1086+25C>G	ENSP00000355897.4:n.1086+25C>G
ENST00000479322.1:n.570+25C>G
NM_001135599.2:c.1170+25C>G	NP_001129071.1:n.1170+25C>G
NM_003238.3:c.1086+25C>G	NP_003229.1:n.1086+25C>G
NM_001135599.3:c.1170+25C>G	NP_001129071.1:n.1170+25C>G
NM_003238.4:c.1086+25C>G	NP_003229.1:n.1086+25C>G
NR_138148.1:n.2389+25C>G
NR_138149.1:n.2473+25C>G
NM_003238.5:c.1086+25C>G	NP_003229.1:n.1086+25C>G
NM_003238.6:c.1086+25C>G MANE Select	NP_003229.1:n.1086+25C>G
NM_001135599.4:c.1170+25C>G	NP_001129071.1:n.1170+25C>G
NR_138148.2:n.2337+25C>G
NR_138149.2:n.2421+25C>G