Canonical Allele Identifier: CA433059045

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30713725G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672233G>T , CM000665.2:g.30672233G>T	GRCh38
NC_000003.11:g.30713725G>T , CM000665.1:g.30713725G>T	GRCh37
NC_000003.10:g.30688729G>T	NCBI36
NG_007490.1:g.70732G>T , LRG_779:g.70732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1050G>T MANE Select	ENSP00000295754.5:p.Leu350=
ENST00000672866.1:n.2646G>T
ENST00000295754.9:c.1050G>T	ENSP00000295754.5:p.Leu350=
ENST00000359013.4:c.1125G>T	ENSP00000351905.4:p.Leu375=
NM_001024847.2:c.1125G>T , LRG_779t1:c.1125G>T	NP_001020018.1:p.Leu375=
NM_003242.5:c.1050G>T	NP_003233.4:p.Leu350=
XM_011534043.1:c.1077G>T	XP_011532345.1:p.Leu359=
XM_011534044.1:c.1002G>T	XP_011532346.1:p.Leu334=
XM_011534045.1:c.945G>T	XP_011532347.1:p.Leu315=
XM_011534043.2:c.1077G>T	XP_011532345.1:p.Leu359=
XM_011534045.3:c.945G>T	XP_011532347.1:p.Leu315=
XM_017007106.1:c.945G>T	XP_016862595.1:p.Leu315=
NM_003242.6:c.1050G>T MANE Select	NP_003233.4:p.Leu350=