Canonical Allele Identifier: CA633470150

Gene: TGFB1 TMEM91

Linked Data

• dbSNP Id: rs139888189
• gnomAD v2: 19-41858561-C-G
• MyVariant Identifiers: chr19:g.41858561C>G (hg19) ; chr19:g.41352656C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352656C>G , CM000681.2:g.41352656C>G	GRCh38
NC_000019.9:g.41858561C>G , CM000681.1:g.41858561C>G	GRCh37
NC_000019.8:g.46550401C>G	NCBI36
NG_013091.1:g.16518G>C
NG_013364.1:g.6271G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.355+34G>C (TGFB1) MANE Select	ENSP00000221930.4:n.355+34G>C
ENST00000600196.2:c.355+34G>C (TGFB1)	ENSP00000504008.1:n.355+34G>C
ENST00000677934.1:c.355+34G>C (TGFB1)	ENSP00000504769.1:n.355+34G>C
ENST00000221930.5:c.355+34G>C (TGFB1)	ENSP00000221930.4:n.355+34G>C
ENST00000539627.5:c.-30+1454C>G (TMEM91)	ENSP00000441900.1:n.-30+1454C>G
ENST00000604424.1:n.350+1454C>G
NM_000660.5:c.355+34G>C (TGFB1)	NP_000651.3:n.355+34G>C
XM_011527242.1:c.355+34G>C (TGFB1)	XP_011525544.1:n.355+34G>C
NM_000660.6:c.355+34G>C (TGFB1)	NP_000651.3:n.355+34G>C
XM_011527242.2:c.355+34G>C (TGFB1)	XP_011525544.1:n.355+34G>C
NM_000660.7:c.355+34G>C (TGFB1) MANE Select	NP_000651.3:n.355+34G>C