Canonical Allele Identifier: CA882328024

Gene: TGFB1 TMEM91

Linked Data

• dbSNP Id: rs1482089489
• gnomAD v3: 19-41353166-C-T
• gnomAD v4: 19-41353166-C-T
• MyVariant Identifiers: chr19:g.41859071C>T (hg19) ; chr19:g.41353166C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41353166C>T , CM000681.2:g.41353166C>T	GRCh38
NC_000019.9:g.41859071C>T , CM000681.1:g.41859071C>T	GRCh37
NC_000019.8:g.46550911C>T	NCBI36
NG_013091.1:g.16008G>A
NG_013364.1:g.5761G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.-122G>A (TGFB1) MANE Select	ENSP00000221930.4:n.-122G>A
ENST00000221930.5:c.-122G>A (TGFB1)	ENSP00000221930.4:n.-122G>A
ENST00000539627.5:c.-30+1964C>T (TMEM91)	ENSP00000441900.1:n.-30+1964C>T
ENST00000604424.1:n.350+1964C>T
NM_000660.5:c.-122G>A (TGFB1)	NP_000651.3:n.-122G>A
XM_011527242.1:c.-122G>A (TGFB1)	XP_011525544.1:n.-122G>A
NM_000660.6:c.-122G>A (TGFB1)	NP_000651.3:n.-122G>A
XM_011527242.2:c.-122G>A (TGFB1)	XP_011525544.1:n.-122G>A
NM_000660.7:c.-122G>A (TGFB1) MANE Select	NP_000651.3:n.-122G>A