Canonical Allele Identifier: CA405999420
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs2038060355

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341950G>T , CM000681.2:g.41341950G>T GRCh38
NC_000019.9:g.41847855G>T , CM000681.1:g.41847855G>T GRCh37
NC_000019.8:g.46539695G>T NCBI36
NG_013364.1:g.16977C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.793C>A MANE Select ENSP00000221930.4:p.Leu265Met
ENST00000600196.2:c.712+220C>A ENSP00000504008.1:n.712+220C>A
ENST00000677934.1:c.634+2797C>A ENSP00000504769.1:n.634+2797C>A
ENST00000221930.5:c.793C>A ENSP00000221930.4:p.Leu265Met
ENST00000598758.5:c.81C>A
ENST00000600196.1:n.172+220C>A
NM_000660.5:c.793C>A NP_000651.3:p.Leu265Met
XM_011527242.1:c.796C>A XP_011525544.1:p.Leu266Met
NM_000660.6:c.793C>A NP_000651.3:p.Leu265Met
XM_011527242.2:c.796C>A XP_011525544.1:p.Leu266Met
NM_000660.7:c.793C>A MANE Select NP_000651.3:p.Leu265Met