Canonical Allele Identifier: CA507689938

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41847856C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341951C>A , CM000681.2:g.41341951C>A	GRCh38
NC_000019.9:g.41847856C>A , CM000681.1:g.41847856C>A	GRCh37
NC_000019.8:g.46539696C>A	NCBI36
NG_013364.1:g.16976G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.792G>T MANE Select	ENSP00000221930.4:p.Pro264=
ENST00000600196.2:c.712+219G>T	ENSP00000504008.1:n.712+219G>T
ENST00000677934.1:c.634+2796G>T	ENSP00000504769.1:n.634+2796G>T
ENST00000221930.5:c.792G>T	ENSP00000221930.4:p.Pro264=
ENST00000598758.5:c.80G>T
ENST00000600196.1:n.172+219G>T
NM_000660.5:c.792G>T	NP_000651.3:p.Pro264=
XM_011527242.1:c.795G>T	XP_011525544.1:p.Pro265=
NM_000660.6:c.792G>T	NP_000651.3:p.Pro264=
XM_011527242.2:c.795G>T	XP_011525544.1:p.Pro265=
NM_000660.7:c.792G>T MANE Select	NP_000651.3:p.Pro264=