Linked Data
ClinVar Variation Id:
1603389
ClinVar RCV Id:
RCV002141997
dbSNP Id:
rs1375130013
gnomAD v4:
19-41352993-G-A
MyVariant Identifiers:
chr19:g.41858898G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41352993G>A , CM000681.2:g.41352993G>A | GRCh38 |
| NC_000019.9:g.41858898G>A , CM000681.1:g.41858898G>A | GRCh37 |
| NC_000019.8:g.46550738G>A | NCBI36 |
| NG_013091.1:g.16181C>T | |
| NG_013364.1:g.5934C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221930.6:c.52C>T (TGFB1) MANE Select | ENSP00000221930.4:p.Leu18= | |
| ENST00000600196.2:c.52C>T (TGFB1) | ENSP00000504008.1:p.Leu18= | |
| ENST00000677934.1:c.52C>T (TGFB1) | ENSP00000504769.1:p.Leu18= | |
| ENST00000221930.5:c.52C>T (TGFB1) | ENSP00000221930.4:p.Leu18= | |
| ENST00000539627.5:c.-30+1791G>A (TMEM91) | ENSP00000441900.1:n.-30+1791G>A | |
| ENST00000604424.1:n.350+1791G>A | ||
| NM_000660.5:c.52C>T (TGFB1) | NP_000651.3:p.Leu18= | |
| XM_011527242.1:c.52C>T (TGFB1) | XP_011525544.1:p.Leu18= | |
| NM_000660.6:c.52C>T (TGFB1) | NP_000651.3:p.Leu18= | |
| XM_011527242.2:c.52C>T (TGFB1) | XP_011525544.1:p.Leu18= | |
| NM_000660.7:c.52C>T (TGFB1) MANE Select | NP_000651.3:p.Leu18= |