Canonical Allele Identifier: CA507689715

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41848148T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342243T>C , CM000681.2:g.41342243T>C	GRCh38
NC_000019.9:g.41848148T>C , CM000681.1:g.41848148T>C	GRCh37
NC_000019.8:g.46539988T>C	NCBI36
NG_013364.1:g.16684A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.639A>G MANE Select	ENSP00000221930.4:p.Glu213=
ENST00000600196.2:c.639A>G	ENSP00000504008.1:p.Glu213=
ENST00000677934.1:c.634+2504A>G	ENSP00000504769.1:n.634+2504A>G
ENST00000221930.5:c.639A>G	ENSP00000221930.4:p.Glu213=
ENST00000597453.1:n.170A>G
ENST00000600196.1:n.99A>G
NM_000660.5:c.639A>G	NP_000651.3:p.Glu213=
XM_011527242.1:c.639A>G	XP_011525544.1:p.Glu213=
NM_000660.6:c.639A>G	NP_000651.3:p.Glu213=
XM_011527242.2:c.639A>G	XP_011525544.1:p.Glu213=
NM_000660.7:c.639A>G MANE Select	NP_000651.3:p.Glu213=