Canonical Allele Identifier: CA1354844281

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30608498G= , CM000665.2:g.30608498G=	GRCh38
NC_000003.11:g.30649990G= , CM000665.1:g.30649990G=	GRCh37
NC_000003.10:g.30624994G=	NCBI36
NG_007490.1:g.6997G= , LRG_779:g.6997G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.94+1521G= MANE Select	ENSP00000295754.5:n.94+1521G=
ENST00000295754.9:c.94+1521G=	ENSP00000295754.5:n.94+1521G=
ENST00000359013.4:c.94+1521G=	ENSP00000351905.4:n.94+1521G=
NM_001024847.2:c.94+1521G= , LRG_779t1:c.94+1521G=	NP_001020018.1:n.94+1521G=
NM_003242.5:c.94+1521G=	NP_003233.4:n.94+1521G=
XM_011534045.1:c.-12+1905G=	XP_011532347.1:n.-12+1905G=
XM_011534045.3:c.-12+1905G=	XP_011532347.1:n.-12+1905G=
NM_003242.6:c.94+1521G= MANE Select	NP_003233.4:n.94+1521G=