HGVS | Genome Assembly |
---|---|
NC_000001.11:g.112956453G>C , CM000663.2:g.112956453G>C | GRCh38 |
NC_000001.10:g.113499075G>C , CM000663.1:g.113499075G>C | GRCh37 |
NC_000001.9:g.113300598G>C | NCBI36 |
NG_015880.2:g.4476C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000429288.2:c.-45+386C>G (SLC16A1) | ENSP00000397106.2:n.-45+386C>G | |
ENST00000679803.1:c.-45+1085C>G (SLC16A1) | ENSP00000505879.1:n.-45+1085C>G | |
ENST00000429288.1:c.-45+386C>G (SLC16A1) | ENSP00000397106.1:n.-45+386C>G | |
NR_103743.1:n.39G>C (SLC16A1-AS1) | ||
NR_103744.1:n.39G>C (SLC16A1-AS1) |