Canonical Allele Identifier: CA507689855

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41847811G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341906G>C , CM000681.2:g.41341906G>C	GRCh38
NC_000019.9:g.41847811G>C , CM000681.1:g.41847811G>C	GRCh37
NC_000019.8:g.46539651G>C	NCBI36
NG_013364.1:g.17021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.837C>G MANE Select	ENSP00000221930.4:p.Ala279=
ENST00000600196.2:c.712+264C>G	ENSP00000504008.1:n.712+264C>G
ENST00000677934.1:c.634+2841C>G	ENSP00000504769.1:n.634+2841C>G
ENST00000221930.5:c.837C>G	ENSP00000221930.4:p.Ala279=
ENST00000598758.5:c.125C>G
ENST00000600196.1:n.172+264C>G
NM_000660.5:c.837C>G	NP_000651.3:p.Ala279=
XM_011527242.1:c.840C>G	XP_011525544.1:p.Ala280=
NM_000660.6:c.837C>G	NP_000651.3:p.Ala279=
XM_011527242.2:c.840C>G	XP_011525544.1:p.Ala280=
NM_000660.7:c.837C>G MANE Select	NP_000651.3:p.Ala279=