Canonical Allele Identifier: CA405998622

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41838150G>T (hg19) ; chr19:g.41332245G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332245G>T , CM000681.2:g.41332245G>T	GRCh38
NC_000019.9:g.41838150G>T , CM000681.1:g.41838150G>T	GRCh37
NC_000019.8:g.46529990G>T	NCBI36
NG_013364.1:g.26682C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.897C>A MANE Select	ENSP00000221930.4:p.Tyr299Ter
ENST00000600196.2:c.749C>A	ENSP00000504008.1:p.Thr250Lys
ENST00000677934.1:c.671C>A	ENSP00000504769.1:p.Thr224Lys
ENST00000221930.5:c.897C>A	ENSP00000221930.4:p.Tyr299Ter
ENST00000598758.5:c.185C>A
ENST00000600196.1:n.209C>A
NM_000660.5:c.897C>A	NP_000651.3:p.Tyr299Ter
XM_011527242.1:c.900C>A	XP_011525544.1:p.Tyr300Ter
NM_000660.6:c.897C>A	NP_000651.3:p.Tyr299Ter
XM_011527242.2:c.900C>A	XP_011525544.1:p.Tyr300Ter
NM_000660.7:c.897C>A MANE Select	NP_000651.3:p.Tyr299Ter