Canonical Allele Identifier: CA507554557

Gene: TGFB1

Linked Data

• dbSNP Id: rs1390467159
• MyVariant Identifiers: chr19:g.41838135C>T (hg19) ; chr19:g.41332230C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332230C>T , CM000681.2:g.41332230C>T	GRCh38
NC_000019.9:g.41838135C>T , CM000681.1:g.41838135C>T	GRCh37
NC_000019.8:g.46529975C>T	NCBI36
NG_013364.1:g.26697G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.912G>A MANE Select	ENSP00000221930.4:p.Lys304=
ENST00000600196.2:c.764G>A	ENSP00000504008.1:p.Arg255Lys
ENST00000677934.1:c.686G>A	ENSP00000504769.1:p.Arg229Lys
ENST00000221930.5:c.912G>A	ENSP00000221930.4:p.Lys304=
ENST00000598758.5:c.200G>A
ENST00000600196.1:n.224G>A
NM_000660.5:c.912G>A	NP_000651.3:p.Lys304=
XM_011527242.1:c.915G>A	XP_011525544.1:p.Lys305=
NM_000660.6:c.912G>A	NP_000651.3:p.Lys304=
XM_011527242.2:c.915G>A	XP_011525544.1:p.Lys305=
NM_000660.7:c.912G>A MANE Select	NP_000651.3:p.Lys304=