Canonical Allele Identifier: CA995968071

Gene: TGFB1

Linked Data

• dbSNP Id: rs2037943793
• gnomAD v3: 19-41332408-C-T
• gnomAD v4: 19-41332408-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332408C>T , CM000681.2:g.41332408C>T	GRCh38
NC_000019.9:g.41838313C>T , CM000681.1:g.41838313C>T	GRCh37
NC_000019.8:g.46530153C>T	NCBI36
NG_013364.1:g.26519G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-127G>A MANE Select	ENSP00000221930.4:n.861-127G>A
ENST00000600196.2:c.713-127G>A	ENSP00000504008.1:n.713-127G>A
ENST00000677934.1:c.635-127G>A	ENSP00000504769.1:n.635-127G>A
ENST00000221930.5:c.861-127G>A	ENSP00000221930.4:n.861-127G>A
ENST00000598758.5:c.149-127G>A
ENST00000600196.1:n.173-127G>A
NM_000660.5:c.861-127G>A	NP_000651.3:n.861-127G>A
XM_011527242.1:c.864-127G>A	XP_011525544.1:n.864-127G>A
NM_000660.6:c.861-127G>A	NP_000651.3:n.861-127G>A
XM_011527242.2:c.864-127G>A	XP_011525544.1:n.864-127G>A
NM_000660.7:c.861-127G>A MANE Select	NP_000651.3:n.861-127G>A