HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24302092_24302093insA , CM000668.2:g.24302092_24302093insA | GRCh38 |
NC_000006.11:g.24302320_24302321insA , CM000668.1:g.24302320_24302321insA | GRCh37 |
NC_000006.10:g.24410299_24410300insA | NCBI36 |
NG_012829.1:g.60960_60961insT | |
NG_012829.2:g.86200_86201insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.349-49_349-48insT MANE Select | ENSP00000367715.3:n.349-49_349-48insT | |
ENST00000378454.7:c.349-49_349-48insT | ENSP00000367715.3:n.349-49_349-48insT | |
NM_001195610.1:c.349-49_349-48insT | NP_001182539.1:n.349-49_349-48insT | |
NM_016356.4:c.349-49_349-48insT | NP_057440.2:n.349-49_349-48insT | |
NM_016356.5:c.349-49_349-48insT MANE Select | NP_057440.2:n.349-49_349-48insT | |
NM_001195610.2:c.349-49_349-48insT | NP_001182539.1:n.349-49_349-48insT |