Canonical Allele Identifier: CA405999281

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41847807C>A (hg19) ; chr19:g.41341902C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341902C>A , CM000681.2:g.41341902C>A	GRCh38
NC_000019.9:g.41847807C>A , CM000681.1:g.41847807C>A	GRCh37
NC_000019.8:g.46539647C>A	NCBI36
NG_013364.1:g.17025G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.841G>T MANE Select	ENSP00000221930.4:p.Asp281Tyr
ENST00000600196.2:c.712+268G>T	ENSP00000504008.1:n.712+268G>T
ENST00000677934.1:c.634+2845G>T	ENSP00000504769.1:n.634+2845G>T
ENST00000221930.5:c.841G>T	ENSP00000221930.4:p.Asp281Tyr
ENST00000598758.5:c.129G>T
ENST00000600196.1:n.172+268G>T
NM_000660.5:c.841G>T	NP_000651.3:p.Asp281Tyr
XM_011527242.1:c.844G>T	XP_011525544.1:p.Asp282Tyr
NM_000660.6:c.841G>T	NP_000651.3:p.Asp281Tyr
XM_011527242.2:c.844G>T	XP_011525544.1:p.Asp282Tyr
NM_000660.7:c.841G>T MANE Select	NP_000651.3:p.Asp281Tyr