HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24302114_24302115delinsAT , CM000668.2:g.24302114_24302115delinsAT | GRCh38 |
NC_000006.11:g.24302342_24302343delinsAT , CM000668.1:g.24302342_24302343delinsAT | GRCh37 |
NC_000006.10:g.24410321_24410322delinsAT | NCBI36 |
NG_012829.1:g.60938_60939delinsAT | |
NG_012829.2:g.86178_86179delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.349-71_349-70delinsAT MANE Select | ENSP00000367715.3:n.349-71_349-70delinsAT | |
ENST00000378454.7:c.349-71_349-70delinsAT | ENSP00000367715.3:n.349-71_349-70delinsAT | |
NM_001195610.1:c.349-71_349-70delinsAT | NP_001182539.1:n.349-71_349-70delinsAT | |
NM_016356.4:c.349-71_349-70delinsAT | NP_057440.2:n.349-71_349-70delinsAT | |
NM_016356.5:c.349-71_349-70delinsAT MANE Select | NP_057440.2:n.349-71_349-70delinsAT | |
NM_001195610.2:c.349-71_349-70delinsAT | NP_001182539.1:n.349-71_349-70delinsAT |