Canonical Allele Identifier: CA196850328

Gene: TGFBR1

Linked Data

• dbSNP Id: rs201607717
• MyVariant Identifiers: chr9:g.101913412A>G (hg19) ; chr9:g.99151130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99151130A>G , CM000671.2:g.99151130A>G	GRCh38
NC_000009.11:g.101913412A>G , CM000671.1:g.101913412A>G	GRCh37
NC_000009.10:g.100953233A>G	NCBI36
NG_007461.1:g.51001A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.*1825A>G	ENSP00000449934.2:n.*1825A>G
ENST00000552573.7:c.*1825A>G	ENSP00000447182.3:n.*1825A>G
ENST00000698941.1:c.*1825A>G	ENSP00000514048.1:n.*1825A>G
ENST00000698943.1:n.2904A>G
ENST00000374994.9:c.*1825A>G MANE Select	ENSP00000364133.4:n.*1825A>G
ENST00000374990.6:c.*1825A>G	ENSP00000364129.2:n.*1825A>G
ENST00000374994.8:c.*1825A>G	ENSP00000364133.4:n.*1825A>G
ENST00000552516.5:c.*1825A>G	ENSP00000447297.1:n.*1825A>G
NM_001130916.1:c.*1825A>G	NP_001124388.1:n.*1825A>G
NM_001130916.2:c.*1825A>G	NP_001124388.1:n.*1825A>G
NM_001306210.1:c.*1825A>G	NP_001293139.1:n.*1825A>G
NM_004612.2:c.*1825A>G	NP_004603.1:n.*1825A>G
NM_004612.3:c.*1825A>G	NP_004603.1:n.*1825A>G
XM_011518948.1:c.*1825A>G	XP_011517250.1:n.*1825A>G
XM_011518949.1:c.*1825A>G	XP_011517251.1:n.*1825A>G
XM_011518950.1:c.*1825A>G	XP_011517252.1:n.*1825A>G
NM_004612.4:c.*1825A>G MANE Select	NP_004603.1:n.*1825A>G
NM_001130916.3:c.*1825A>G	NP_001124388.1:n.*1825A>G
NM_001306210.2:c.*1825A>G	NP_001293139.1:n.*1825A>G