Canonical Allele Identifier: CA405998757

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41838185A>G (hg19) ; chr19:g.41332280A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332280A>G , CM000681.2:g.41332280A>G	GRCh38
NC_000019.9:g.41838185A>G , CM000681.1:g.41838185A>G	GRCh37
NC_000019.8:g.46530025A>G	NCBI36
NG_013364.1:g.26647T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.862T>C MANE Select	ENSP00000221930.4:p.Ser288Pro
ENST00000600196.2:c.714T>C	ENSP00000504008.1:p.Ala238=
ENST00000677934.1:c.636T>C	ENSP00000504769.1:p.Ala212=
ENST00000221930.5:c.862T>C	ENSP00000221930.4:p.Ser288Pro
ENST00000598758.5:c.150T>C
ENST00000600196.1:n.174T>C
NM_000660.5:c.862T>C	NP_000651.3:p.Ser288Pro
XM_011527242.1:c.865T>C	XP_011525544.1:p.Ser289Pro
NM_000660.6:c.862T>C	NP_000651.3:p.Ser288Pro
XM_011527242.2:c.865T>C	XP_011525544.1:p.Ser289Pro
NM_000660.7:c.862T>C MANE Select	NP_000651.3:p.Ser288Pro