Canonical Allele Identifier: CA1221565892

Gene: TGFB2

Linked Data

• dbSNP Id: rs1659999353
• gnomAD v4: 1-218437265-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437265T>G , CM000663.2:g.218437265T>G	GRCh38
NC_000001.10:g.218610607T>G , CM000663.1:g.218610607T>G	GRCh37
NC_000001.9:g.216677230T>G	NCBI36
NG_027721.1:g.96932T>G
NG_027721.2:g.96932T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-78T>G MANE Select	ENSP00000355897.4:n.933-78T>G
ENST00000366929.4:c.1017-78T>G	ENSP00000355896.4:n.1017-78T>G
ENST00000366930.8:c.933-78T>G	ENSP00000355897.4:n.933-78T>G
ENST00000479322.1:n.417-78T>G
NM_001135599.2:c.1017-78T>G	NP_001129071.1:n.1017-78T>G
NM_003238.3:c.933-78T>G	NP_003229.1:n.933-78T>G
NM_001135599.3:c.1017-78T>G	NP_001129071.1:n.1017-78T>G
NM_003238.4:c.933-78T>G	NP_003229.1:n.933-78T>G
NR_138148.1:n.2236-78T>G
NR_138149.1:n.2320-78T>G
NM_003238.5:c.933-78T>G	NP_003229.1:n.933-78T>G
NM_003238.6:c.933-78T>G MANE Select	NP_003229.1:n.933-78T>G
NM_001135599.4:c.1017-78T>G	NP_001129071.1:n.1017-78T>G
NR_138148.2:n.2184-78T>G
NR_138149.2:n.2268-78T>G