Canonical Allele Identifier: CA351806411

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30644803T>C , CM000665.2:g.30644803T>C	GRCh38
NC_000003.11:g.30686295T>C , CM000665.1:g.30686295T>C	GRCh37
NC_000003.10:g.30661299T>C	NCBI36
NG_007490.1:g.43302T>C , LRG_779:g.43302T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.151T>C MANE Select	NP_003233.4:p.Cys51Arg
ENST00000295754.10:c.151T>C MANE Select	ENSP00000295754.5:p.Cys51Arg
NM_001024847.2:c.226T>C , LRG_779t1:c.226T>C	NP_001020018.1:p.Cys76Arg
NM_003242.5:c.151T>C	NP_003233.4:p.Cys51Arg
ENST00000295754.9:c.151T>C	ENSP00000295754.5:p.Cys51Arg
ENST00000359013.4:c.226T>C	ENSP00000351905.4:p.Cys76Arg
ENST00000672866.1:n.1747T>C
ENST00000673250.1:n.275T>C
XM_011534043.1:c.178T>C	XP_011532345.1:p.Cys60Arg
XM_011534043.2:c.178T>C	XP_011532345.1:p.Cys60Arg
XM_011534044.1:c.103T>C	XP_011532346.1:p.Cys35Arg
XM_011534045.1:c.46T>C	XP_011532347.1:p.Cys16Arg
XM_011534045.3:c.46T>C	XP_011532347.1:p.Cys16Arg
XM_017007106.1:c.46T>C	XP_016862595.1:p.Cys16Arg