Canonical Allele Identifier: CA351807563

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30713322G>C (hg19) ; chr3:g.30671830G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671830G>C , CM000665.2:g.30671830G>C	GRCh38
NC_000003.11:g.30713322G>C , CM000665.1:g.30713322G>C	GRCh37
NC_000003.10:g.30688326G>C	NCBI36
NG_007490.1:g.70329G>C , LRG_779:g.70329G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.647G>C MANE Select	ENSP00000295754.5:p.Cys216Ser
ENST00000672866.1:n.2243G>C
ENST00000295754.9:c.647G>C	ENSP00000295754.5:p.Cys216Ser
ENST00000359013.4:c.722G>C	ENSP00000351905.4:p.Cys241Ser
NM_001024847.2:c.722G>C , LRG_779t1:c.722G>C	NP_001020018.1:p.Cys241Ser
NM_003242.5:c.647G>C	NP_003233.4:p.Cys216Ser
XM_011534043.1:c.674G>C	XP_011532345.1:p.Cys225Ser
XM_011534044.1:c.599G>C	XP_011532346.1:p.Cys200Ser
XM_011534045.1:c.542G>C	XP_011532347.1:p.Cys181Ser
XM_011534043.2:c.674G>C	XP_011532345.1:p.Cys225Ser
XM_011534045.3:c.542G>C	XP_011532347.1:p.Cys181Ser
XM_017007106.1:c.542G>C	XP_016862595.1:p.Cys181Ser
NM_003242.6:c.647G>C MANE Select	NP_003233.4:p.Cys216Ser