Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.112956698C>A , CM000663.2:g.112956698C>A | GRCh38 |
| NC_000001.10:g.113499320C>A , CM000663.1:g.113499320C>A | GRCh37 |
| NC_000001.9:g.113300843C>A | NCBI36 |
| NG_015880.2:g.4231G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_103743.1:n.284C>A (SLC16A1-AS1) | |
| NR_103744.1:n.284C>A (SLC16A1-AS1) | |
| ENST00000429288.1:c.-45+141G>T (SLC16A1) | ENSP00000397106.1:n.-45+141G>T |
| ENST00000429288.2:c.-45+141G>T (SLC16A1) | ENSP00000397106.2:n.-45+141G>T |
| ENST00000679803.1:c.-45+840G>T (SLC16A1) | ENSP00000505879.1:n.-45+840G>T |