Canonical Allele Identifier: CA2336421171
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1568477932

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342290C>G , CM000681.2:g.41342290C>G GRCh38
NC_000019.9:g.41848195C>G , CM000681.1:g.41848195C>G GRCh37
NC_000019.8:g.46540035C>G NCBI36
NG_013364.1:g.16637G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-43G>C MANE Select ENSP00000221930.4:n.635-43G>C
ENST00000600196.2:c.635-43G>C ENSP00000504008.1:n.635-43G>C
ENST00000677934.1:c.634+2457G>C ENSP00000504769.1:n.634+2457G>C
ENST00000221930.5:c.635-43G>C ENSP00000221930.4:n.635-43G>C
ENST00000597453.1:n.166-43G>C
ENST00000600196.1:n.95-43G>C
NM_000660.5:c.635-43G>C NP_000651.3:n.635-43G>C
XM_011527242.1:c.635-43G>C XP_011525544.1:n.635-43G>C
NM_000660.6:c.635-43G>C NP_000651.3:n.635-43G>C
XM_011527242.2:c.635-43G>C XP_011525544.1:n.635-43G>C
NM_000660.7:c.635-43G>C MANE Select NP_000651.3:n.635-43G>C