Canonical Allele Identifier: CA406004907

Gene: TGFB1 TMEM91

Linked Data

• MyVariant Identifiers: chr19:g.41858627A>G (hg19) ; chr19:g.41352722A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352722A>G , CM000681.2:g.41352722A>G	GRCh38
NC_000019.9:g.41858627A>G , CM000681.1:g.41858627A>G	GRCh37
NC_000019.8:g.46550467A>G	NCBI36
NG_013091.1:g.16452T>C
NG_013364.1:g.6205T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.323T>C (TGFB1) MANE Select	ENSP00000221930.4:p.Val108Ala
ENST00000600196.2:c.323T>C (TGFB1)	ENSP00000504008.1:p.Val108Ala
ENST00000677934.1:c.323T>C (TGFB1)	ENSP00000504769.1:p.Val108Ala
ENST00000221930.5:c.323T>C (TGFB1)	ENSP00000221930.4:p.Val108Ala
ENST00000539627.5:c.-30+1520A>G (TMEM91)	ENSP00000441900.1:n.-30+1520A>G
ENST00000604424.1:n.350+1520A>G
NM_000660.5:c.323T>C (TGFB1)	NP_000651.3:p.Val108Ala
XM_011527242.1:c.323T>C (TGFB1)	XP_011525544.1:p.Val108Ala
NM_000660.6:c.323T>C (TGFB1)	NP_000651.3:p.Val108Ala
XM_011527242.2:c.323T>C (TGFB1)	XP_011525544.1:p.Val108Ala
NM_000660.7:c.323T>C (TGFB1) MANE Select	NP_000651.3:p.Val108Ala