Canonical Allele Identifier: CA351807979

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125434599
• MyVariant Identifiers: chr3:g.30713513C>T (hg19) ; chr3:g.30672021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672021C>T , CM000665.2:g.30672021C>T	GRCh38
NC_000003.11:g.30713513C>T , CM000665.1:g.30713513C>T	GRCh37
NC_000003.10:g.30688517C>T	NCBI36
NG_007490.1:g.70520C>T , LRG_779:g.70520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.838C>T MANE Select	ENSP00000295754.5:p.Pro280Ser
ENST00000672866.1:n.2434C>T
ENST00000295754.9:c.838C>T	ENSP00000295754.5:p.Pro280Ser
ENST00000359013.4:c.913C>T	ENSP00000351905.4:p.Pro305Ser
NM_001024847.2:c.913C>T , LRG_779t1:c.913C>T	NP_001020018.1:p.Pro305Ser
NM_003242.5:c.838C>T	NP_003233.4:p.Pro280Ser
XM_011534043.1:c.865C>T	XP_011532345.1:p.Pro289Ser
XM_011534044.1:c.790C>T	XP_011532346.1:p.Pro264Ser
XM_011534045.1:c.733C>T	XP_011532347.1:p.Pro245Ser
XM_011534043.2:c.865C>T	XP_011532345.1:p.Pro289Ser
XM_011534045.3:c.733C>T	XP_011532347.1:p.Pro245Ser
XM_017007106.1:c.733C>T	XP_016862595.1:p.Pro245Ser
NM_003242.6:c.838C>T MANE Select	NP_003233.4:p.Pro280Ser