HGVS | Genome Assembly |
---|---|
NC_000019.10:g.918616C>T , CM000681.2:g.918616C>T | GRCh38 |
NC_000019.9:g.918616C>T , CM000681.1:g.918616C>T | GRCh37 |
NC_000019.8:g.869616C>T | NCBI36 |
NG_008277.1:g.6275C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234371.10:c.317C>T MANE Select | ENSP00000234371.3:p.Pro106Leu | |
ENST00000234371.9:c.317C>T | ENSP00000234371.3:p.Pro106Leu | |
ENST00000592648.1:c.244+870C>T | ENSP00000467666.1:n.244+870C>T | |
ENST00000606939.2:c.317C>T | ENSP00000475639.1:p.Pro106Leu | |
NM_032551.4:c.317C>T | NP_115940.2:p.Pro106Leu | |
XM_017027382.1:c.317C>T | XP_016882871.1:p.Pro106Leu | |
NM_032551.5:c.317C>T MANE Select | NP_115940.2:p.Pro106Leu |