Canonical Allele Identifier: CA308515302
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348306C>T , CM000681.2:g.41348306C>T GRCh38
NC_000019.9:g.41854211C>T , CM000681.1:g.41854211C>T GRCh37
NC_000019.8:g.46546051C>T NCBI36
NG_013364.1:g.10621G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.505G>A MANE Select ENSP00000221930.4:p.Glu169Lys
ENST00000600196.2:c.505G>A ENSP00000504008.1:p.Glu169Lys
ENST00000677934.1:c.505G>A ENSP00000504769.1:p.Glu169Lys
ENST00000221930.5:c.505G>A ENSP00000221930.4:p.Glu169Lys
ENST00000597453.1:n.36G>A
NM_000660.5:c.505G>A NP_000651.3:p.Glu169Lys
XM_011527242.1:c.505G>A XP_011525544.1:p.Glu169Lys
NM_000660.6:c.505G>A NP_000651.3:p.Glu169Lys
XM_011527242.2:c.505G>A XP_011525544.1:p.Glu169Lys
NM_000660.7:c.505G>A MANE Select NP_000651.3:p.Glu169Lys