Linked Data
MyVariant Identifiers:
chr1:g.218518642G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218345300G>T , CM000663.2:g.218345300G>T | GRCh38 |
| NC_000001.10:g.218518642G>T , CM000663.1:g.218518642G>T | GRCh37 |
| NC_000001.9:g.216585265G>T | NCBI36 |
| NG_027721.1:g.4967G>T | |
| NG_027721.2:g.4967G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046268.1:n.165C>A (TGFB2-AS1) | ||
| NM_001135599.3:c.-1402G>T (TGFB2) | NP_001129071.1:n.-1402G>T | |
| NM_003238.4:c.-1402G>T (TGFB2) | NP_003229.1:n.-1402G>T | |
| NR_138148.1:n.17G>T (TGFB2) | ||
| NR_138149.1:n.17G>T (TGFB2) |