HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186933A>T , CM000669.2:g.98186933A>T | GRCh38 |
NC_000007.13:g.97816245A>T , CM000669.1:g.97816245A>T | GRCh37 |
NC_000007.12:g.97654181A>T | NCBI36 |
NG_013375.1:g.85049A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.933A>T MANE Select | ENSP00000297293.5:p.Pro311= | |
ENST00000297293.5:c.933A>T | ENSP00000297293.5:p.Pro311= | |
NM_014916.3:c.933A>T | NP_055731.2:p.Pro311= | |
XM_011515981.1:c.927A>T | XP_011514283.1:p.Pro309= | |
XM_011515981.3:c.927A>T | XP_011514283.1:p.Pro309= | |
NM_014916.4:c.933A>T MANE Select | NP_055731.2:p.Pro311= |