Canonical Allele Identifier: CA344725872

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218578522C>A (hg19) ; chr1:g.218405180C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405180C>A , CM000663.2:g.218405180C>A	GRCh38
NC_000001.10:g.218578522C>A , CM000663.1:g.218578522C>A	GRCh37
NC_000001.9:g.216645145C>A	NCBI36
NG_027721.1:g.64847C>A
NG_027721.2:g.64847C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.358C>A MANE Select	ENSP00000355897.4:p.Pro120Thr
ENST00000366929.4:c.442C>A	ENSP00000355896.4:p.Pro148Thr
ENST00000366930.8:c.358C>A	ENSP00000355897.4:p.Pro120Thr
ENST00000488793.1:n.22C>A
NM_001135599.2:c.442C>A	NP_001129071.1:p.Pro148Thr
NM_003238.3:c.358C>A	NP_003229.1:p.Pro120Thr
NM_001135599.3:c.442C>A	NP_001129071.1:p.Pro148Thr
NM_003238.4:c.358C>A	NP_003229.1:p.Pro120Thr
NR_138148.1:n.1776C>A
NR_138149.1:n.1860C>A
NM_003238.5:c.358C>A	NP_003229.1:p.Pro120Thr
NM_003238.6:c.358C>A MANE Select	NP_003229.1:p.Pro120Thr
NM_001135599.4:c.442C>A	NP_001129071.1:p.Pro148Thr
NR_138148.2:n.1724C>A
NR_138149.2:n.1808C>A