Canonical Allele Identifier: CA2336426331
Gene: TGFB1 HGNC NCBI
TMEM91 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41353212A= , CM000681.2:g.41353212A= GRCh38
NC_000019.9:g.41859117A= , CM000681.1:g.41859117A= GRCh37
NC_000019.8:g.46550957A= NCBI36
NG_013091.1:g.15962T=
NG_013364.1:g.5715T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.-168T= (TGFB1) MANE Select ENSP00000221930.4:n.-168T=
ENST00000221930.5:c.-168T= (TGFB1) ENSP00000221930.4:n.-168T=
ENST00000539627.5:c.-30+2010A= (TMEM91) ENSP00000441900.1:n.-30+2010A=
ENST00000604424.1:n.350+2010A=
NM_000660.5:c.-168T= (TGFB1) NP_000651.3:n.-168T=
XM_011527242.1:c.-168T= (TGFB1) XP_011525544.1:n.-168T=
NM_000660.6:c.-168T= (TGFB1) NP_000651.3:n.-168T=
XM_011527242.2:c.-168T= (TGFB1) XP_011525544.1:n.-168T=
NM_000660.7:c.-168T= (TGFB1) MANE Select NP_000651.3:n.-168T=
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