Canonical Allele Identifier: CA351808380

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30713697T>C (hg19) ; chr3:g.30672205T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672205T>C , CM000665.2:g.30672205T>C	GRCh38
NC_000003.11:g.30713697T>C , CM000665.1:g.30713697T>C	GRCh37
NC_000003.10:g.30688701T>C	NCBI36
NG_007490.1:g.70704T>C , LRG_779:g.70704T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1022T>C MANE Select	ENSP00000295754.5:p.Val341Ala
ENST00000672866.1:n.2618T>C
ENST00000295754.9:c.1022T>C	ENSP00000295754.5:p.Val341Ala
ENST00000359013.4:c.1097T>C	ENSP00000351905.4:p.Val366Ala
NM_001024847.2:c.1097T>C , LRG_779t1:c.1097T>C	NP_001020018.1:p.Val366Ala
NM_003242.5:c.1022T>C	NP_003233.4:p.Val341Ala
XM_011534043.1:c.1049T>C	XP_011532345.1:p.Val350Ala
XM_011534044.1:c.974T>C	XP_011532346.1:p.Val325Ala
XM_011534045.1:c.917T>C	XP_011532347.1:p.Val306Ala
XM_011534043.2:c.1049T>C	XP_011532345.1:p.Val350Ala
XM_011534045.3:c.917T>C	XP_011532347.1:p.Val306Ala
XM_017007106.1:c.917T>C	XP_016862595.1:p.Val306Ala
NM_003242.6:c.1022T>C MANE Select	NP_003233.4:p.Val341Ala