Canonical Allele Identifier: CA405999715

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342026-G-T
• MyVariant Identifiers: chr19:g.41847931G>T (hg19) ; chr19:g.41342026G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342026G>T , CM000681.2:g.41342026G>T	GRCh38
NC_000019.9:g.41847931G>T , CM000681.1:g.41847931G>T	GRCh37
NC_000019.8:g.46539771G>T	NCBI36
NG_013364.1:g.16901C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.717C>A MANE Select	ENSP00000221930.4:p.Phe239Leu
ENST00000600196.2:c.712+144C>A	ENSP00000504008.1:n.712+144C>A
ENST00000677934.1:c.634+2721C>A	ENSP00000504769.1:n.634+2721C>A
ENST00000221930.5:c.717C>A	ENSP00000221930.4:p.Phe239Leu
ENST00000597453.1:n.387C>A
ENST00000598758.5:c.5C>A
ENST00000600196.1:n.172+144C>A
NM_000660.5:c.717C>A	NP_000651.3:p.Phe239Leu
XM_011527242.1:c.720C>A	XP_011525544.1:p.Phe240Leu
NM_000660.6:c.717C>A	NP_000651.3:p.Phe239Leu
XM_011527242.2:c.720C>A	XP_011525544.1:p.Phe240Leu
NM_000660.7:c.717C>A MANE Select	NP_000651.3:p.Phe239Leu