Canonical Allele Identifier: CA045560

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672249C>T , CM000665.2:g.30672249C>T	GRCh38
NC_000003.11:g.30713741C>T , CM000665.1:g.30713741C>T	GRCh37
NC_000003.10:g.30688745C>T	NCBI36
NG_007490.1:g.70748C>T , LRG_779:g.70748C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1066C>T MANE Select	NP_003233.4:p.Arg356Trp
ENST00000295754.10:c.1066C>T MANE Select	ENSP00000295754.5:p.Arg356Trp
NM_001024847.2:c.1141C>T , LRG_779t1:c.1141C>T	NP_001020018.1:p.Arg381Trp
NM_003242.5:c.1066C>T	NP_003233.4:p.Arg356Trp
ENST00000295754.9:c.1066C>T	ENSP00000295754.5:p.Arg356Trp
ENST00000359013.4:c.1141C>T	ENSP00000351905.4:p.Arg381Trp
ENST00000672866.1:n.2662C>T
XM_011534043.1:c.1093C>T	XP_011532345.1:p.Arg365Trp
XM_011534043.2:c.1093C>T	XP_011532345.1:p.Arg365Trp
XM_011534044.1:c.1018C>T	XP_011532346.1:p.Arg340Trp
XM_011534045.1:c.961C>T	XP_011532347.1:p.Arg321Trp
XM_011534045.3:c.961C>T	XP_011532347.1:p.Arg321Trp
XM_017007106.1:c.961C>T	XP_016862595.1:p.Arg321Trp