Canonical Allele Identifier: CA344725881

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218578526C>T (hg19) ; chr1:g.218405184C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405184C>T , CM000663.2:g.218405184C>T	GRCh38
NC_000001.10:g.218578526C>T , CM000663.1:g.218578526C>T	GRCh37
NC_000001.9:g.216645149C>T	NCBI36
NG_027721.1:g.64851C>T
NG_027721.2:g.64851C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.362C>T MANE Select	ENSP00000355897.4:p.Thr121Ile
ENST00000366929.4:c.446C>T	ENSP00000355896.4:p.Thr149Ile
ENST00000366930.8:c.362C>T	ENSP00000355897.4:p.Thr121Ile
ENST00000488793.1:n.26C>T
NM_001135599.2:c.446C>T	NP_001129071.1:p.Thr149Ile
NM_003238.3:c.362C>T	NP_003229.1:p.Thr121Ile
NM_001135599.3:c.446C>T	NP_001129071.1:p.Thr149Ile
NM_003238.4:c.362C>T	NP_003229.1:p.Thr121Ile
NR_138148.1:n.1780C>T
NR_138149.1:n.1864C>T
NM_003238.5:c.362C>T	NP_003229.1:p.Thr121Ile
NM_003238.6:c.362C>T MANE Select	NP_003229.1:p.Thr121Ile
NM_001135599.4:c.446C>T	NP_001129071.1:p.Thr149Ile
NR_138148.2:n.1728C>T
NR_138149.2:n.1812C>T