Canonical Allele Identifier: CA1354881676

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691462C= , CM000665.2:g.30691462C=	GRCh38
NC_000003.11:g.30732954C= , CM000665.1:g.30732954C=	GRCh37
NC_000003.10:g.30707958C=	NCBI36
NG_007490.1:g.89961C= , LRG_779:g.89961C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1567C= MANE Select	ENSP00000295754.5:p.His523=
ENST00000672050.1:n.451C=
ENST00000672866.1:n.3163C=
ENST00000673203.1:n.445C=
ENST00000295754.9:c.1567C=	ENSP00000295754.5:p.His523=
ENST00000359013.4:c.1642C=	ENSP00000351905.4:p.His548=
NM_001024847.2:c.1642C= , LRG_779t1:c.1642C=	NP_001020018.1:p.His548=
NM_003242.5:c.1567C=	NP_003233.4:p.His523=
XM_011534043.1:c.1594C=	XP_011532345.1:p.His532=
XM_011534044.1:c.1519C=	XP_011532346.1:p.His507=
XM_011534045.1:c.1462C=	XP_011532347.1:p.His488=
XM_011534043.2:c.1594C=	XP_011532345.1:p.His532=
XM_011534045.3:c.1462C=	XP_011532347.1:p.His488=
XM_017007106.1:c.1462C=	XP_016862595.1:p.His488=
NM_003242.6:c.1567C= MANE Select	NP_003233.4:p.His523=