Canonical Allele Identifier: CA432917700

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30715623A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674131A>C , CM000665.2:g.30674131A>C	GRCh38
NC_000003.11:g.30715623A>C , CM000665.1:g.30715623A>C	GRCh37
NC_000003.10:g.30690627A>C	NCBI36
NG_007490.1:g.72630A>C , LRG_779:g.72630A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1281A>C MANE Select	ENSP00000295754.5:p.Pro427=
ENST00000672866.1:n.2877A>C
ENST00000673203.1:n.159A>C
ENST00000295754.9:c.1281A>C	ENSP00000295754.5:p.Pro427=
ENST00000359013.4:c.1356A>C	ENSP00000351905.4:p.Pro452=
NM_001024847.2:c.1356A>C , LRG_779t1:c.1356A>C	NP_001020018.1:p.Pro452=
NM_003242.5:c.1281A>C	NP_003233.4:p.Pro427=
XM_011534043.1:c.1308A>C	XP_011532345.1:p.Pro436=
XM_011534044.1:c.1233A>C	XP_011532346.1:p.Pro411=
XM_011534045.1:c.1176A>C	XP_011532347.1:p.Pro392=
XM_011534043.2:c.1308A>C	XP_011532345.1:p.Pro436=
XM_011534045.3:c.1176A>C	XP_011532347.1:p.Pro392=
XM_017007106.1:c.1176A>C	XP_016862595.1:p.Pro392=
NM_003242.6:c.1281A>C MANE Select	NP_003233.4:p.Pro427=