Canonical Allele Identifier: CA432917698

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30715620T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674128T>C , CM000665.2:g.30674128T>C	GRCh38
NC_000003.11:g.30715620T>C , CM000665.1:g.30715620T>C	GRCh37
NC_000003.10:g.30690624T>C	NCBI36
NG_007490.1:g.72627T>C , LRG_779:g.72627T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1278T>C MANE Select	ENSP00000295754.5:p.Ala426=
ENST00000672866.1:n.2874T>C
ENST00000673203.1:n.156T>C
ENST00000295754.9:c.1278T>C	ENSP00000295754.5:p.Ala426=
ENST00000359013.4:c.1353T>C	ENSP00000351905.4:p.Ala451=
NM_001024847.2:c.1353T>C , LRG_779t1:c.1353T>C	NP_001020018.1:p.Ala451=
NM_003242.5:c.1278T>C	NP_003233.4:p.Ala426=
XM_011534043.1:c.1305T>C	XP_011532345.1:p.Ala435=
XM_011534044.1:c.1230T>C	XP_011532346.1:p.Ala410=
XM_011534045.1:c.1173T>C	XP_011532347.1:p.Ala391=
XM_011534043.2:c.1305T>C	XP_011532345.1:p.Ala435=
XM_011534045.3:c.1173T>C	XP_011532347.1:p.Ala391=
XM_017007106.1:c.1173T>C	XP_016862595.1:p.Ala391=
NM_003242.6:c.1278T>C MANE Select	NP_003233.4:p.Ala426=