Canonical Allele Identifier: CA1221568503

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660152047
• gnomAD v4: 1-218441532-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441532G>A , CM000663.2:g.218441532G>A	GRCh38
NC_000001.10:g.218614874G>A , CM000663.1:g.218614874G>A	GRCh37
NC_000001.9:g.216681497G>A	NCBI36
NG_027721.1:g.101199G>A
NG_027721.2:g.101199G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*170G>A MANE Select	ENSP00000355897.4:n.*170G>A
ENST00000366929.4:c.*170G>A	ENSP00000355896.4:n.*170G>A
ENST00000366930.8:c.*170G>A	ENSP00000355897.4:n.*170G>A
ENST00000479322.1:n.899G>A
NM_001135599.2:c.*170G>A	NP_001129071.1:n.*170G>A
NM_003238.3:c.*170G>A	NP_003229.1:n.*170G>A
NM_001135599.3:c.*170G>A	NP_001129071.1:n.*170G>A
NM_003238.4:c.*170G>A	NP_003229.1:n.*170G>A
NR_138148.1:n.2718G>A
NR_138149.1:n.2802G>A
NM_003238.5:c.*170G>A	NP_003229.1:n.*170G>A
NM_003238.6:c.*170G>A MANE Select	NP_003229.1:n.*170G>A
NM_001135599.4:c.*170G>A	NP_001129071.1:n.*170G>A
NR_138148.2:n.2666G>A
NR_138149.2:n.2750G>A