Canonical Allele Identifier: CA2336423775
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41347988T= , CM000681.2:g.41347988T= GRCh38
NC_000019.9:g.41853893T= , CM000681.1:g.41853893T= GRCh37
NC_000019.8:g.46545733T= NCBI36
NG_013364.1:g.10939A=

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.516+307A= MANE Select ENSP00000221930.4:n.516+307A=
ENST00000600196.2:c.516+307A= ENSP00000504008.1:n.516+307A=
ENST00000677934.1:c.516+307A= ENSP00000504769.1:n.516+307A=
ENST00000221930.5:c.516+307A= ENSP00000221930.4:n.516+307A=
ENST00000597453.1:n.47+307A=
NM_000660.5:c.516+307A= NP_000651.3:n.516+307A=
XM_011527242.1:c.516+307A= XP_011525544.1:n.516+307A=
NM_000660.6:c.516+307A= NP_000651.3:n.516+307A=
XM_011527242.2:c.516+307A= XP_011525544.1:n.516+307A=
NM_000660.7:c.516+307A= MANE Select NP_000651.3:n.516+307A=