Canonical Allele Identifier: CA1221568335

Gene: TGFB2

Linked Data

• dbSNP Id: rs1660137500
• gnomAD v4: 1-218441159-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441159T>G , CM000663.2:g.218441159T>G	GRCh38
NC_000001.10:g.218614501T>G , CM000663.1:g.218614501T>G	GRCh37
NC_000001.9:g.216681124T>G	NCBI36
NG_027721.1:g.100826T>G
NG_027721.2:g.100826T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1087-45T>G MANE Select	ENSP00000355897.4:n.1087-45T>G
ENST00000366929.4:c.1171-45T>G	ENSP00000355896.4:n.1171-45T>G
ENST00000366930.8:c.1087-45T>G	ENSP00000355897.4:n.1087-45T>G
ENST00000479322.1:n.571-45T>G
NM_001135599.2:c.1171-45T>G	NP_001129071.1:n.1171-45T>G
NM_003238.3:c.1087-45T>G	NP_003229.1:n.1087-45T>G
NM_001135599.3:c.1171-45T>G	NP_001129071.1:n.1171-45T>G
NM_003238.4:c.1087-45T>G	NP_003229.1:n.1087-45T>G
NR_138148.1:n.2390-45T>G
NR_138149.1:n.2474-45T>G
NM_003238.5:c.1087-45T>G	NP_003229.1:n.1087-45T>G
NM_003238.6:c.1087-45T>G MANE Select	NP_003229.1:n.1087-45T>G
NM_001135599.4:c.1171-45T>G	NP_001129071.1:n.1171-45T>G
NR_138148.2:n.2338-45T>G
NR_138149.2:n.2422-45T>G