Canonical Allele Identifier: CA344726727

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218607683G>A (hg19) ; chr1:g.218434341G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434341G>A , CM000663.2:g.218434341G>A	GRCh38
NC_000001.10:g.218607683G>A , CM000663.1:g.218607683G>A	GRCh37
NC_000001.9:g.216674306G>A	NCBI36
NG_027721.1:g.94008G>A
NG_027721.2:g.94008G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.647G>A MANE Select	ENSP00000355897.4:p.Arg216Lys
ENST00000366929.4:c.731G>A	ENSP00000355896.4:p.Arg244Lys
ENST00000366930.8:c.647G>A	ENSP00000355897.4:p.Arg216Lys
ENST00000479322.1:n.131G>A
NM_001135599.2:c.731G>A	NP_001129071.1:p.Arg244Lys
NM_003238.3:c.647G>A	NP_003229.1:p.Arg216Lys
NM_001135599.3:c.731G>A	NP_001129071.1:p.Arg244Lys
NM_003238.4:c.647G>A	NP_003229.1:p.Arg216Lys
NR_138148.1:n.2065G>A
NR_138149.1:n.2149G>A
NM_003238.5:c.647G>A	NP_003229.1:p.Arg216Lys
NM_003238.6:c.647G>A MANE Select	NP_003229.1:p.Arg216Lys
NM_001135599.4:c.731G>A	NP_001129071.1:p.Arg244Lys
NR_138148.2:n.2013G>A
NR_138149.2:n.2097G>A