Canonical Allele Identifier: CA2562888501
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41337502C>G , CM000681.2:g.41337502C>G GRCh38
NC_000019.9:g.41843407C>G , CM000681.1:g.41843407C>G GRCh37
NC_000019.8:g.46535247C>G NCBI36
NG_013364.1:g.21425G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.860+4381G>C MANE Select ENSP00000221930.4:n.860+4381G>C
ENST00000600196.2:c.712+4668G>C ENSP00000504008.1:n.712+4668G>C
ENST00000677934.1:c.635-5221G>C ENSP00000504769.1:n.635-5221G>C
ENST00000221930.5:c.860+4381G>C ENSP00000221930.4:n.860+4381G>C
ENST00000598758.5:c.148+4381G>C
ENST00000600196.1:n.172+4668G>C
NM_000660.5:c.860+4381G>C NP_000651.3:n.860+4381G>C
XM_011527242.1:c.863+4381G>C XP_011525544.1:n.863+4381G>C
NM_000660.6:c.860+4381G>C NP_000651.3:n.860+4381G>C
XM_011527242.2:c.863+4381G>C XP_011525544.1:n.863+4381G>C
NM_000660.7:c.860+4381G>C MANE Select NP_000651.3:n.860+4381G>C