Canonical Allele Identifier: CA351808676

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1049576348
• MyVariant Identifiers: chr3:g.30713841A>C (hg19) ; chr3:g.30672349A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672349A>C , CM000665.2:g.30672349A>C	GRCh38
NC_000003.11:g.30713841A>C , CM000665.1:g.30713841A>C	GRCh37
NC_000003.10:g.30688845A>C	NCBI36
NG_007490.1:g.70848A>C , LRG_779:g.70848A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1166A>C MANE Select	ENSP00000295754.5:p.Asn389Thr
ENST00000672866.1:n.2762A>C
ENST00000295754.9:c.1166A>C	ENSP00000295754.5:p.Asn389Thr
ENST00000359013.4:c.1241A>C	ENSP00000351905.4:p.Asn414Thr
NM_001024847.2:c.1241A>C , LRG_779t1:c.1241A>C	NP_001020018.1:p.Asn414Thr
NM_003242.5:c.1166A>C	NP_003233.4:p.Asn389Thr
XM_011534043.1:c.1193A>C	XP_011532345.1:p.Asn398Thr
XM_011534044.1:c.1118A>C	XP_011532346.1:p.Asn373Thr
XM_011534045.1:c.1061A>C	XP_011532347.1:p.Asn354Thr
XM_011534043.2:c.1193A>C	XP_011532345.1:p.Asn398Thr
XM_011534045.3:c.1061A>C	XP_011532347.1:p.Asn354Thr
XM_017007106.1:c.1061A>C	XP_016862595.1:p.Asn354Thr
NM_003242.6:c.1166A>C MANE Select	NP_003233.4:p.Asn389Thr