HGVS | Genome Assembly |
---|---|
NC_000023.11:g.29917359T>C , CM000685.2:g.29917359T>C | GRCh38 |
NC_000023.10:g.29935476T>C , CM000685.1:g.29935476T>C | GRCh37 |
NC_000023.9:g.29845397T>C | NCBI36 |
NG_008292.1:g.1334796T>C | |
NG_008292.2:g.1334796T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378993.6:c.779-105T>C MANE Select | ENSP00000368278.1:n.779-105T>C | |
ENST00000378993.5:c.779-105T>C | ENSP00000368278.1:n.779-105T>C | |
NM_014271.3:c.779-105T>C | NP_055086.1:n.779-105T>C | |
XM_005274441.1:c.779-105T>C | XP_005274498.1:n.779-105T>C | |
XM_011545445.1:c.779-105T>C | XP_011543747.1:n.779-105T>C | |
XM_017029240.1:c.779-105T>C | XP_016884729.1:n.779-105T>C | |
XM_017029241.1:c.401-105T>C | XP_016884730.1:n.401-105T>C | |
NM_014271.4:c.779-105T>C MANE Select | NP_055086.1:n.779-105T>C |