Canonical Allele Identifier: CA351806534

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30644854A>T , CM000665.2:g.30644854A>T	GRCh38
NC_000003.11:g.30686346A>T , CM000665.1:g.30686346A>T	GRCh37
NC_000003.10:g.30661350A>T	NCBI36
NG_007490.1:g.43353A>T , LRG_779:g.43353A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.202A>T MANE Select	NP_003233.4:p.Met68Leu
ENST00000295754.10:c.202A>T MANE Select	ENSP00000295754.5:p.Met68Leu
NM_001024847.2:c.277A>T , LRG_779t1:c.277A>T	NP_001020018.1:p.Met93Leu
NM_003242.5:c.202A>T	NP_003233.4:p.Met68Leu
ENST00000295754.9:c.202A>T	ENSP00000295754.5:p.Met68Leu
ENST00000359013.4:c.277A>T	ENSP00000351905.4:p.Met93Leu
ENST00000672866.1:n.1798A>T
ENST00000673250.1:n.326A>T
XM_011534043.1:c.229A>T	XP_011532345.1:p.Met77Leu
XM_011534043.2:c.229A>T	XP_011532345.1:p.Met77Leu
XM_011534044.1:c.154A>T	XP_011532346.1:p.Met52Leu
XM_011534045.1:c.97A>T	XP_011532347.1:p.Met33Leu
XM_011534045.3:c.97A>T	XP_011532347.1:p.Met33Leu
XM_017007106.1:c.97A>T	XP_016862595.1:p.Met33Leu