Canonical Allele Identifier: CA405998467

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41838101C>G (hg19) ; chr19:g.41332196C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332196C>G , CM000681.2:g.41332196C>G	GRCh38
NC_000019.9:g.41838101C>G , CM000681.1:g.41838101C>G	GRCh37
NC_000019.8:g.46529941C>G	NCBI36
NG_013364.1:g.26731G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.946G>C MANE Select	ENSP00000221930.4:p.Gly316Arg
ENST00000600196.2:c.798G>C	ENSP00000504008.1:p.Arg266Ser
ENST00000677934.1:c.720G>C	ENSP00000504769.1:p.Arg240Ser
ENST00000221930.5:c.946G>C	ENSP00000221930.4:p.Gly316Arg
ENST00000598758.5:c.234G>C
ENST00000600196.1:n.258G>C
NM_000660.5:c.946G>C	NP_000651.3:p.Gly316Arg
XM_011527242.1:c.949G>C	XP_011525544.1:p.Gly317Arg
NM_000660.6:c.946G>C	NP_000651.3:p.Gly316Arg
XM_011527242.2:c.949G>C	XP_011525544.1:p.Gly317Arg
NM_000660.7:c.946G>C MANE Select	NP_000651.3:p.Gly316Arg