Canonical Allele Identifier: CA344725870

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218578520C>A (hg19) ; chr1:g.218405178C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405178C>A , CM000663.2:g.218405178C>A	GRCh38
NC_000001.10:g.218578520C>A , CM000663.1:g.218578520C>A	GRCh37
NC_000001.9:g.216645143C>A	NCBI36
NG_027721.1:g.64845C>A
NG_027721.2:g.64845C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.356C>A MANE Select	ENSP00000355897.4:p.Pro119Gln
ENST00000366929.4:c.440C>A	ENSP00000355896.4:p.Pro147Gln
ENST00000366930.8:c.356C>A	ENSP00000355897.4:p.Pro119Gln
ENST00000488793.1:n.20C>A
NM_001135599.2:c.440C>A	NP_001129071.1:p.Pro147Gln
NM_003238.3:c.356C>A	NP_003229.1:p.Pro119Gln
NM_001135599.3:c.440C>A	NP_001129071.1:p.Pro147Gln
NM_003238.4:c.356C>A	NP_003229.1:p.Pro119Gln
NR_138148.1:n.1774C>A
NR_138149.1:n.1858C>A
NM_003238.5:c.356C>A	NP_003229.1:p.Pro119Gln
NM_003238.6:c.356C>A MANE Select	NP_003229.1:p.Pro119Gln
NM_001135599.4:c.440C>A	NP_001129071.1:p.Pro147Gln
NR_138148.2:n.1722C>A
NR_138149.2:n.1806C>A