Canonical Allele Identifier: CA2336416596
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs2037944977

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332514A>G , CM000681.2:g.41332514A>G GRCh38
NC_000019.9:g.41838419A>G , CM000681.1:g.41838419A>G GRCh37
NC_000019.8:g.46530259A>G NCBI36
NG_013364.1:g.26413T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-233T>C MANE Select ENSP00000221930.4:n.861-233T>C
ENST00000600196.2:c.713-233T>C ENSP00000504008.1:n.713-233T>C
ENST00000677934.1:c.635-233T>C ENSP00000504769.1:n.635-233T>C
ENST00000221930.5:c.861-233T>C ENSP00000221930.4:n.861-233T>C
ENST00000598758.5:c.149-233T>C
ENST00000600196.1:n.173-233T>C
NM_000660.5:c.861-233T>C NP_000651.3:n.861-233T>C
XM_011527242.1:c.864-233T>C XP_011525544.1:n.864-233T>C
NM_000660.6:c.861-233T>C NP_000651.3:n.861-233T>C
XM_011527242.2:c.864-233T>C XP_011525544.1:n.864-233T>C
NM_000660.7:c.861-233T>C MANE Select NP_000651.3:n.861-233T>C