Canonical Allele Identifier: CA2585296353

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41341879-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341879T>C , CM000681.2:g.41341879T>C	GRCh38
NC_000019.9:g.41847784T>C , CM000681.1:g.41847784T>C	GRCh37
NC_000019.8:g.46539624T>C	NCBI36
NG_013364.1:g.17048A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.860+4A>G MANE Select	ENSP00000221930.4:n.860+4A>G
ENST00000600196.2:c.712+291A>G	ENSP00000504008.1:n.712+291A>G
ENST00000677934.1:c.634+2868A>G	ENSP00000504769.1:n.634+2868A>G
ENST00000221930.5:c.860+4A>G	ENSP00000221930.4:n.860+4A>G
ENST00000598758.5:c.148+4A>G
ENST00000600196.1:n.172+291A>G
NM_000660.5:c.860+4A>G	NP_000651.3:n.860+4A>G
XM_011527242.1:c.863+4A>G	XP_011525544.1:n.863+4A>G
NM_000660.6:c.860+4A>G	NP_000651.3:n.860+4A>G
XM_011527242.2:c.863+4A>G	XP_011525544.1:n.863+4A>G
NM_000660.7:c.860+4A>G MANE Select	NP_000651.3:n.860+4A>G