Canonical Allele Identifier: CA196852338

Gene: TGFBR1

Linked Data

• dbSNP Id: rs988548471
• MyVariant Identifiers: chr9:g.101915938G>A (hg19) ; chr9:g.99153656G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99153656G>A , CM000671.2:g.99153656G>A	GRCh38
NC_000009.11:g.101915938G>A , CM000671.1:g.101915938G>A	GRCh37
NC_000009.10:g.100955759G>A	NCBI36
NG_007461.1:g.53527G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.*4351G>A	ENSP00000449934.2:n.*4351G>A
ENST00000552573.7:c.*4351G>A	ENSP00000447182.3:n.*4351G>A
ENST00000374994.9:c.*4351G>A MANE Select	ENSP00000364133.4:n.*4351G>A
ENST00000374994.8:c.*4351G>A	ENSP00000364133.4:n.*4351G>A
ENST00000552516.5:c.*4351G>A	ENSP00000447297.1:n.*4351G>A
NM_001130916.1:c.*4351G>A	NP_001124388.1:n.*4351G>A
NM_001130916.2:c.*4351G>A	NP_001124388.1:n.*4351G>A
NM_001306210.1:c.*4351G>A	NP_001293139.1:n.*4351G>A
NM_004612.2:c.*4351G>A	NP_004603.1:n.*4351G>A
NM_004612.3:c.*4351G>A	NP_004603.1:n.*4351G>A
XM_011518948.1:c.*4351G>A	XP_011517250.1:n.*4351G>A
XM_011518949.1:c.*4351G>A	XP_011517251.1:n.*4351G>A
XM_011518950.1:c.*4351G>A	XP_011517252.1:n.*4351G>A
NM_004612.4:c.*4351G>A MANE Select	NP_004603.1:n.*4351G>A
NM_001130916.3:c.*4351G>A	NP_001124388.1:n.*4351G>A
NM_001306210.2:c.*4351G>A	NP_001293139.1:n.*4351G>A