Canonical Allele Identifier: CA351807862

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30713460A>T (hg19) ; chr3:g.30671968A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30671968A>T , CM000665.2:g.30671968A>T	GRCh38
NC_000003.11:g.30713460A>T , CM000665.1:g.30713460A>T	GRCh37
NC_000003.10:g.30688464A>T	NCBI36
NG_007490.1:g.70467A>T , LRG_779:g.70467A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.785A>T MANE Select	ENSP00000295754.5:p.Lys262Met
ENST00000672866.1:n.2381A>T
ENST00000295754.9:c.785A>T	ENSP00000295754.5:p.Lys262Met
ENST00000359013.4:c.860A>T	ENSP00000351905.4:p.Lys287Met
NM_001024847.2:c.860A>T , LRG_779t1:c.860A>T	NP_001020018.1:p.Lys287Met
NM_003242.5:c.785A>T	NP_003233.4:p.Lys262Met
XM_011534043.1:c.812A>T	XP_011532345.1:p.Lys271Met
XM_011534044.1:c.737A>T	XP_011532346.1:p.Lys246Met
XM_011534045.1:c.680A>T	XP_011532347.1:p.Lys227Met
XM_011534043.2:c.812A>T	XP_011532345.1:p.Lys271Met
XM_011534045.3:c.680A>T	XP_011532347.1:p.Lys227Met
XM_017007106.1:c.680A>T	XP_016862595.1:p.Lys227Met
NM_003242.6:c.785A>T MANE Select	NP_003233.4:p.Lys262Met