Canonical Allele Identifier: CA049464

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671822C>T , CM000665.2:g.30671822C>T	GRCh38
NC_000003.11:g.30713314C>T , CM000665.1:g.30713314C>T	GRCh37
NC_000003.10:g.30688318C>T	NCBI36
NG_007490.1:g.70321C>T , LRG_779:g.70321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.639C>T MANE Select	ENSP00000295754.5:p.Ser213=
ENST00000672866.1:n.2235C>T
ENST00000295754.9:c.639C>T	ENSP00000295754.5:p.Ser213=
ENST00000359013.4:c.714C>T	ENSP00000351905.4:p.Ser238=
NM_001024847.2:c.714C>T , LRG_779t1:c.714C>T	NP_001020018.1:p.Ser238=
NM_003242.5:c.639C>T	NP_003233.4:p.Ser213=
XM_011534043.1:c.666C>T	XP_011532345.1:p.Ser222=
XM_011534044.1:c.591C>T	XP_011532346.1:p.Ser197=
XM_011534045.1:c.534C>T	XP_011532347.1:p.Ser178=
XM_011534043.2:c.666C>T	XP_011532345.1:p.Ser222=
XM_011534045.3:c.534C>T	XP_011532347.1:p.Ser178=
XM_017007106.1:c.534C>T	XP_016862595.1:p.Ser178=
NM_003242.6:c.639C>T MANE Select	NP_003233.4:p.Ser213=