Canonical Allele Identifier: CA351808640

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1699358635
• MyVariant Identifiers: chr3:g.30713822T>C (hg19) ; chr3:g.30672330T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672330T>C , CM000665.2:g.30672330T>C	GRCh38
NC_000003.11:g.30713822T>C , CM000665.1:g.30713822T>C	GRCh37
NC_000003.10:g.30688826T>C	NCBI36
NG_007490.1:g.70829T>C , LRG_779:g.70829T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1147T>C MANE Select	ENSP00000295754.5:p.Ser383Pro
ENST00000672866.1:n.2743T>C
ENST00000295754.9:c.1147T>C	ENSP00000295754.5:p.Ser383Pro
ENST00000359013.4:c.1222T>C	ENSP00000351905.4:p.Ser408Pro
NM_001024847.2:c.1222T>C , LRG_779t1:c.1222T>C	NP_001020018.1:p.Ser408Pro
NM_003242.5:c.1147T>C	NP_003233.4:p.Ser383Pro
XM_011534043.1:c.1174T>C	XP_011532345.1:p.Ser392Pro
XM_011534044.1:c.1099T>C	XP_011532346.1:p.Ser367Pro
XM_011534045.1:c.1042T>C	XP_011532347.1:p.Ser348Pro
XM_011534043.2:c.1174T>C	XP_011532345.1:p.Ser392Pro
XM_011534045.3:c.1042T>C	XP_011532347.1:p.Ser348Pro
XM_017007106.1:c.1042T>C	XP_016862595.1:p.Ser348Pro
NM_003242.6:c.1147T>C MANE Select	NP_003233.4:p.Ser383Pro