Canonical Allele Identifier: CA995955722

Gene: TGFB1

Linked Data

• dbSNP Id: rs2038068173
• gnomAD v3: 19-41342391-T-C
• gnomAD v4: 19-41342391-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342391T>C , CM000681.2:g.41342391T>C	GRCh38
NC_000019.9:g.41848296T>C , CM000681.1:g.41848296T>C	GRCh37
NC_000019.8:g.46540136T>C	NCBI36
NG_013364.1:g.16536A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-144A>G MANE Select	ENSP00000221930.4:n.635-144A>G
ENST00000600196.2:c.635-144A>G	ENSP00000504008.1:n.635-144A>G
ENST00000677934.1:c.634+2356A>G	ENSP00000504769.1:n.634+2356A>G
ENST00000221930.5:c.635-144A>G	ENSP00000221930.4:n.635-144A>G
ENST00000597453.1:n.166-144A>G
ENST00000600196.1:n.95-144A>G
NM_000660.5:c.635-144A>G	NP_000651.3:n.635-144A>G
XM_011527242.1:c.635-144A>G	XP_011525544.1:n.635-144A>G
NM_000660.6:c.635-144A>G	NP_000651.3:n.635-144A>G
XM_011527242.2:c.635-144A>G	XP_011525544.1:n.635-144A>G
NM_000660.7:c.635-144A>G MANE Select	NP_000651.3:n.635-144A>G