Canonical Allele Identifier: CA406003452
Gene: TGFB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348300A>T , CM000681.2:g.41348300A>T GRCh38
NC_000019.9:g.41854205A>T , CM000681.1:g.41854205A>T GRCh37
NC_000019.8:g.46546045A>T NCBI36
NG_013364.1:g.10627T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.511T>A MANE Select ENSP00000221930.4:p.Tyr171Asn
ENST00000600196.2:c.511T>A ENSP00000504008.1:p.Tyr171Asn
ENST00000677934.1:c.511T>A ENSP00000504769.1:p.Tyr171Asn
ENST00000221930.5:c.511T>A ENSP00000221930.4:p.Tyr171Asn
ENST00000597453.1:n.42T>A
NM_000660.5:c.511T>A NP_000651.3:p.Tyr171Asn
XM_011527242.1:c.511T>A XP_011525544.1:p.Tyr171Asn
NM_000660.6:c.511T>A NP_000651.3:p.Tyr171Asn
XM_011527242.2:c.511T>A XP_011525544.1:p.Tyr171Asn
NM_000660.7:c.511T>A MANE Select NP_000651.3:p.Tyr171Asn