HGVS | Genome Assembly |
---|---|
NC_000001.11:g.84399670T>C , CM000663.2:g.84399670T>C | GRCh38 |
NC_000001.10:g.84865353T>C , CM000663.1:g.84865353T>C | GRCh37 |
NC_000001.9:g.84637941T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370665.4:c.125+981T>C MANE Select | ENSP00000359699.3:n.125+981T>C | |
ENST00000370665.3:c.125+981T>C | ENSP00000359699.3:n.125+981T>C | |
NM_021233.2:c.125+981T>C | NP_067056.2:n.125+981T>C | |
NM_021233.3:c.125+981T>C MANE Select | NP_067056.2:n.125+981T>C |