Canonical Allele Identifier: CA2336420969
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341892T= , CM000681.2:g.41341892T= GRCh38
NC_000019.9:g.41847797T= , CM000681.1:g.41847797T= GRCh37
NC_000019.8:g.46539637T= NCBI36
NG_013364.1:g.17035A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.851A= MANE Select ENSP00000221930.4:p.Tyr284=
ENST00000600196.2:c.712+278A= ENSP00000504008.1:n.712+278A=
ENST00000677934.1:c.634+2855A= ENSP00000504769.1:n.634+2855A=
ENST00000221930.5:c.851A= ENSP00000221930.4:p.Tyr284=
ENST00000598758.5:c.139A=
ENST00000600196.1:n.172+278A=
NM_000660.5:c.851A= NP_000651.3:p.Tyr284=
XM_011527242.1:c.854A= XP_011525544.1:p.Tyr285=
NM_000660.6:c.851A= NP_000651.3:p.Tyr284=
XM_011527242.2:c.854A= XP_011525544.1:p.Tyr285=
NM_000660.7:c.851A= MANE Select NP_000651.3:p.Tyr284=