Canonical Allele Identifier: CA351808970

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30715646A>C (hg19) ; chr3:g.30674154A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674154A>C , CM000665.2:g.30674154A>C	GRCh38
NC_000003.11:g.30715646A>C , CM000665.1:g.30715646A>C	GRCh37
NC_000003.10:g.30690650A>C	NCBI36
NG_007490.1:g.72653A>C , LRG_779:g.72653A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1304A>C MANE Select	ENSP00000295754.5:p.Asn435Thr
ENST00000672866.1:n.2900A>C
ENST00000673203.1:n.182A>C
ENST00000295754.9:c.1304A>C	ENSP00000295754.5:p.Asn435Thr
ENST00000359013.4:c.1379A>C	ENSP00000351905.4:p.Asn460Thr
NM_001024847.2:c.1379A>C , LRG_779t1:c.1379A>C	NP_001020018.1:p.Asn460Thr
NM_003242.5:c.1304A>C	NP_003233.4:p.Asn435Thr
XM_011534043.1:c.1331A>C	XP_011532345.1:p.Asn444Thr
XM_011534044.1:c.1256A>C	XP_011532346.1:p.Asn419Thr
XM_011534045.1:c.1199A>C	XP_011532347.1:p.Asn400Thr
XM_011534043.2:c.1331A>C	XP_011532345.1:p.Asn444Thr
XM_011534045.3:c.1199A>C	XP_011532347.1:p.Asn400Thr
XM_017007106.1:c.1199A>C	XP_016862595.1:p.Asn400Thr
NM_003242.6:c.1304A>C MANE Select	NP_003233.4:p.Asn435Thr