Canonical Allele Identifier: CA405999338

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41847836A>C (hg19) ; chr19:g.41341931A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341931A>C , CM000681.2:g.41341931A>C	GRCh38
NC_000019.9:g.41847836A>C , CM000681.1:g.41847836A>C	GRCh37
NC_000019.8:g.46539676A>C	NCBI36
NG_013364.1:g.16996T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.812T>G MANE Select	ENSP00000221930.4:p.Leu271Arg
ENST00000600196.2:c.712+239T>G	ENSP00000504008.1:n.712+239T>G
ENST00000677934.1:c.634+2816T>G	ENSP00000504769.1:n.634+2816T>G
ENST00000221930.5:c.812T>G	ENSP00000221930.4:p.Leu271Arg
ENST00000598758.5:c.100T>G
ENST00000600196.1:n.172+239T>G
NM_000660.5:c.812T>G	NP_000651.3:p.Leu271Arg
XM_011527242.1:c.815T>G	XP_011525544.1:p.Leu272Arg
NM_000660.6:c.812T>G	NP_000651.3:p.Leu271Arg
XM_011527242.2:c.815T>G	XP_011525544.1:p.Leu272Arg
NM_000660.7:c.812T>G MANE Select	NP_000651.3:p.Leu271Arg