Canonical Allele Identifier: CA2336421097
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342147A= , CM000681.2:g.41342147A= GRCh38
NC_000019.9:g.41848052A= , CM000681.1:g.41848052A= GRCh37
NC_000019.8:g.46539892A= NCBI36
NG_013364.1:g.16780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.712+23T= MANE Select ENSP00000221930.4:n.712+23T=
ENST00000600196.2:c.712+23T= ENSP00000504008.1:n.712+23T=
ENST00000677934.1:c.634+2600T= ENSP00000504769.1:n.634+2600T=
ENST00000221930.5:c.712+23T= ENSP00000221930.4:n.712+23T=
ENST00000597453.1:n.266T=
ENST00000600196.1:n.172+23T=
NM_000660.5:c.712+23T= NP_000651.3:n.712+23T=
XM_011527242.1:c.712+23T= XP_011525544.1:n.712+23T=
NM_000660.6:c.712+23T= NP_000651.3:n.712+23T=
XM_011527242.2:c.712+23T= XP_011525544.1:n.712+23T=
NM_000660.7:c.712+23T= MANE Select NP_000651.3:n.712+23T=