Canonical Allele Identifier: CA351809498

Gene: TGFBR2

Linked Data

• MyVariant Identifiers: chr3:g.30732922T>G (hg19) ; chr3:g.30691430T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691430T>G , CM000665.2:g.30691430T>G	GRCh38
NC_000003.11:g.30732922T>G , CM000665.1:g.30732922T>G	GRCh37
NC_000003.10:g.30707926T>G	NCBI36
NG_007490.1:g.89929T>G , LRG_779:g.89929T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1535T>G MANE Select	ENSP00000295754.5:p.Met512Arg
ENST00000672050.1:n.419T>G
ENST00000672866.1:n.3131T>G
ENST00000673203.1:n.413T>G
ENST00000295754.9:c.1535T>G	ENSP00000295754.5:p.Met512Arg
ENST00000359013.4:c.1610T>G	ENSP00000351905.4:p.Met537Arg
NM_001024847.2:c.1610T>G , LRG_779t1:c.1610T>G	NP_001020018.1:p.Met537Arg
NM_003242.5:c.1535T>G	NP_003233.4:p.Met512Arg
XM_011534043.1:c.1562T>G	XP_011532345.1:p.Met521Arg
XM_011534044.1:c.1487T>G	XP_011532346.1:p.Met496Arg
XM_011534045.1:c.1430T>G	XP_011532347.1:p.Met477Arg
XM_011534043.2:c.1562T>G	XP_011532345.1:p.Met521Arg
XM_011534045.3:c.1430T>G	XP_011532347.1:p.Met477Arg
XM_017007106.1:c.1430T>G	XP_016862595.1:p.Met477Arg
NM_003242.6:c.1535T>G MANE Select	NP_003233.4:p.Met512Arg