Canonical Allele Identifier: CA2585296219

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41332382-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332382C>G , CM000681.2:g.41332382C>G	GRCh38
NC_000019.9:g.41838287C>G , CM000681.1:g.41838287C>G	GRCh37
NC_000019.8:g.46530127C>G	NCBI36
NG_013364.1:g.26545G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-101G>C MANE Select	ENSP00000221930.4:n.861-101G>C
ENST00000600196.2:c.713-101G>C	ENSP00000504008.1:n.713-101G>C
ENST00000677934.1:c.635-101G>C	ENSP00000504769.1:n.635-101G>C
ENST00000221930.5:c.861-101G>C	ENSP00000221930.4:n.861-101G>C
ENST00000598758.5:c.149-101G>C
ENST00000600196.1:n.173-101G>C
NM_000660.5:c.861-101G>C	NP_000651.3:n.861-101G>C
XM_011527242.1:c.864-101G>C	XP_011525544.1:n.864-101G>C
NM_000660.6:c.861-101G>C	NP_000651.3:n.861-101G>C
XM_011527242.2:c.864-101G>C	XP_011525544.1:n.864-101G>C
NM_000660.7:c.861-101G>C MANE Select	NP_000651.3:n.861-101G>C