Canonical Allele Identifier: CA10618027

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30692042A>G , CM000665.2:g.30692042A>G	GRCh38
NC_000003.11:g.30733534A>G , CM000665.1:g.30733534A>G	GRCh37
NC_000003.10:g.30708538A>G	NCBI36
NG_007490.1:g.90541A>G , LRG_779:g.90541A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.*443A>G MANE Select	NP_003233.4:n.*443A>G
ENST00000295754.10:c.*443A>G MANE Select	ENSP00000295754.5:n.*443A>G
NM_001024847.2:c.*443A>G , LRG_779t1:c.*443A>G	NP_001020018.1:n.*443A>G
NM_003242.5:c.*443A>G	NP_003233.4:n.*443A>G
ENST00000295754.9:c.*443A>G	ENSP00000295754.5:n.*443A>G
ENST00000359013.4:c.*443A>G	ENSP00000351905.4:n.*443A>G
ENST00000672866.1:n.3743A>G
ENST00000673203.1:n.1025A>G
XM_011534043.1:c.*443A>G	XP_011532345.1:n.*443A>G
XM_011534043.2:c.*443A>G	XP_011532345.1:n.*443A>G
XM_011534044.1:c.*443A>G	XP_011532346.1:n.*443A>G
XM_011534045.1:c.*443A>G	XP_011532347.1:n.*443A>G
XM_011534045.3:c.*443A>G	XP_011532347.1:n.*443A>G
XM_017007106.1:c.*443A>G	XP_016862595.1:n.*443A>G