Canonical Allele Identifier: CA1354843281

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606887G= , CM000665.2:g.30606887G=	GRCh38
NC_000003.11:g.30648379G= , CM000665.1:g.30648379G=	GRCh37
NC_000003.10:g.30623383G=	NCBI36
NG_007490.1:g.5386G= , LRG_779:g.5386G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.4G= MANE Select	ENSP00000295754.5:p.Gly2=
ENST00000295754.9:c.4G=	ENSP00000295754.5:p.Gly2=
ENST00000359013.4:c.4G=	ENSP00000351905.4:p.Gly2=
NM_001024847.2:c.4G= , LRG_779t1:c.4G=	NP_001020018.1:p.Gly2=
NM_003242.5:c.4G=	NP_003233.4:p.Gly2=
XM_011534045.1:c.-12+294G=	XP_011532347.1:n.-12+294G=
XM_011534045.3:c.-12+294G=	XP_011532347.1:n.-12+294G=
NM_003242.6:c.4G= MANE Select	NP_003233.4:p.Gly2=