Canonical Allele Identifier: CA2582167002
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs2123099232

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342350C>A , CM000681.2:g.41342350C>A GRCh38
NC_000019.9:g.41848255C>A , CM000681.1:g.41848255C>A GRCh37
NC_000019.8:g.46540095C>A NCBI36
NG_013364.1:g.16577G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-103G>T MANE Select ENSP00000221930.4:n.635-103G>T
ENST00000600196.2:c.635-103G>T ENSP00000504008.1:n.635-103G>T
ENST00000677934.1:c.634+2397G>T ENSP00000504769.1:n.634+2397G>T
ENST00000221930.5:c.635-103G>T ENSP00000221930.4:n.635-103G>T
ENST00000597453.1:n.166-103G>T
ENST00000600196.1:n.95-103G>T
NM_000660.5:c.635-103G>T NP_000651.3:n.635-103G>T
XM_011527242.1:c.635-103G>T XP_011525544.1:n.635-103G>T
NM_000660.6:c.635-103G>T NP_000651.3:n.635-103G>T
XM_011527242.2:c.635-103G>T XP_011525544.1:n.635-103G>T
NM_000660.7:c.635-103G>T MANE Select NP_000651.3:n.635-103G>T