Canonical Allele Identifier: CA406006406

Gene: TGFB1 TMEM91

Linked Data

• gnomAD v4: 19-41352996-A-G
• MyVariant Identifiers: chr19:g.41858901A>G (hg19) ; chr19:g.41352996A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352996A>G , CM000681.2:g.41352996A>G	GRCh38
NC_000019.9:g.41858901A>G , CM000681.1:g.41858901A>G	GRCh37
NC_000019.8:g.46550741A>G	NCBI36
NG_013091.1:g.16178T>C
NG_013364.1:g.5931T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.49T>C (TGFB1) MANE Select	ENSP00000221930.4:p.Trp17Arg
ENST00000600196.2:c.49T>C (TGFB1)	ENSP00000504008.1:p.Trp17Arg
ENST00000677934.1:c.49T>C (TGFB1)	ENSP00000504769.1:p.Trp17Arg
ENST00000221930.5:c.49T>C (TGFB1)	ENSP00000221930.4:p.Trp17Arg
ENST00000539627.5:c.-30+1794A>G (TMEM91)	ENSP00000441900.1:n.-30+1794A>G
ENST00000604424.1:n.350+1794A>G
NM_000660.5:c.49T>C (TGFB1)	NP_000651.3:p.Trp17Arg
XM_011527242.1:c.49T>C (TGFB1)	XP_011525544.1:p.Trp17Arg
NM_000660.6:c.49T>C (TGFB1)	NP_000651.3:p.Trp17Arg
XM_011527242.2:c.49T>C (TGFB1)	XP_011525544.1:p.Trp17Arg
NM_000660.7:c.49T>C (TGFB1) MANE Select	NP_000651.3:p.Trp17Arg