Canonical Allele Identifier: CA11592424

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30641455T>C , CM000665.2:g.30641455T>C	GRCh38
NC_000003.11:g.30682947T>C , CM000665.1:g.30682947T>C	GRCh37
NC_000003.10:g.30657951T>C	NCBI36
NG_007490.1:g.39954T>C , LRG_779:g.39954T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.95-3292T>C MANE Select	NP_003233.4:n.95-3292T>C
ENST00000295754.10:c.95-3292T>C MANE Select	ENSP00000295754.5:n.95-3292T>C
NM_001024847.2:c.170-3292T>C , LRG_779t1:c.170-3292T>C	NP_001020018.1:n.170-3292T>C
NM_003242.5:c.95-3292T>C	NP_003233.4:n.95-3292T>C
ENST00000295754.9:c.95-3292T>C	ENSP00000295754.5:n.95-3292T>C
ENST00000359013.4:c.170-3292T>C	ENSP00000351905.4:n.170-3292T>C
ENST00000672866.1:n.1691-3292T>C
ENST00000673250.1:n.219-3292T>C
XM_011534043.1:c.122-3292T>C	XP_011532345.1:n.122-3292T>C
XM_011534043.2:c.122-3292T>C	XP_011532345.1:n.122-3292T>C
XM_011534044.1:c.47-3292T>C	XP_011532346.1:n.47-3292T>C
XM_011534045.1:c.-11-3292T>C	XP_011532347.1:n.-11-3292T>C
XM_011534045.3:c.-11-3292T>C	XP_011532347.1:n.-11-3292T>C
XM_017007106.1:c.-11-3292T>C	XP_016862595.1:n.-11-3292T>C