Canonical Allele Identifier: CA995964138
Gene: TGFB1 HGNC NCBI
TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs1840922641

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41353146A>G , CM000681.2:g.41353146A>G GRCh38
NC_000019.9:g.41859051A>G , CM000681.1:g.41859051A>G GRCh37
NC_000019.8:g.46550891A>G NCBI36
NG_013091.1:g.16028T>C
NG_013364.1:g.5781T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.-102T>C (TGFB1) MANE Select ENSP00000221930.4:n.-102T>C
ENST00000221930.5:c.-102T>C (TGFB1) ENSP00000221930.4:n.-102T>C
ENST00000539627.5:c.-30+1944A>G (TMEM91) ENSP00000441900.1:n.-30+1944A>G
ENST00000604424.1:n.350+1944A>G
NM_000660.5:c.-102T>C (TGFB1) NP_000651.3:n.-102T>C
XM_011527242.1:c.-102T>C (TGFB1) XP_011525544.1:n.-102T>C
NM_000660.6:c.-102T>C (TGFB1) NP_000651.3:n.-102T>C
XM_011527242.2:c.-102T>C (TGFB1) XP_011525544.1:n.-102T>C
NM_000660.7:c.-102T>C (TGFB1) MANE Select NP_000651.3:n.-102T>C