HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173121G>T , CM000678.2:g.173121G>T | GRCh38 |
NC_000016.9:g.223120G>T , CM000678.1:g.223120G>T | GRCh37 |
NC_000016.8:g.163120G>T | NCBI36 |
NG_000006.1:g.33984G>T | |
NG_059186.1:g.1471G>T | |
NG_059271.1:g.5275G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251595.11:c.96-4G>T MANE Select | ENSP00000251595.6:n.96-4G>T | |
ENST00000251595.10:c.96-4G>T | ENSP00000251595.6:n.96-4G>T | |
ENST00000397806.1:c.-1-4G>T | ENSP00000380908.1:n.-1-4G>T | |
ENST00000482565.1:n.228G>T | ||
ENST00000484216.1:n.65-4G>T | ||
NM_000517.4:c.96-4G>T | NP_000508.1:n.96-4G>T | |
NM_000517.6:c.96-4G>T MANE Select | NP_000508.1:n.96-4G>T |