Canonical Allele Identifier: CA308563116

Gene: TGFB1

Linked Data

• dbSNP Id: rs1033475386
• MyVariant Identifiers: chr19:g.41838382C>G (hg19) ; chr19:g.41332477C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332477C>G , CM000681.2:g.41332477C>G	GRCh38
NC_000019.9:g.41838382C>G , CM000681.1:g.41838382C>G	GRCh37
NC_000019.8:g.46530222C>G	NCBI36
NG_013364.1:g.26450G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-196G>C MANE Select	ENSP00000221930.4:n.861-196G>C
ENST00000600196.2:c.713-196G>C	ENSP00000504008.1:n.713-196G>C
ENST00000677934.1:c.635-196G>C	ENSP00000504769.1:n.635-196G>C
ENST00000221930.5:c.861-196G>C	ENSP00000221930.4:n.861-196G>C
ENST00000598758.5:c.149-196G>C
ENST00000600196.1:n.173-196G>C
NM_000660.5:c.861-196G>C	NP_000651.3:n.861-196G>C
XM_011527242.1:c.864-196G>C	XP_011525544.1:n.864-196G>C
NM_000660.6:c.861-196G>C	NP_000651.3:n.861-196G>C
XM_011527242.2:c.864-196G>C	XP_011525544.1:n.864-196G>C
NM_000660.7:c.861-196G>C MANE Select	NP_000651.3:n.861-196G>C