HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31139544_31139553del , CM000668.2:g.31139544_31139553del | GRCh38 |
NC_000006.11:g.31107321_31107330del , CM000668.1:g.31107321_31107330del | GRCh37 |
NC_000006.10:g.31215300_31215309del | NCBI36 |
NG_021348.1:g.29714_29723del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.168-97_168-88del MANE Select | ENSP00000259881.9:n.168-97_168-88del | |
ENST00000259881.9:c.168-97_168-88del | ENSP00000259881.9:n.168-97_168-88del | |
ENST00000479581.5:n.62-97_62-88del | ||
ENST00000481450.2:c.-22-97_-22-88del | ENSP00000447158.1:n.-22-97_-22-88del | |
ENST00000547221.1:c.24-97_24-88del | ENSP00000449471.1:n.24-97_24-88del | |
NM_014068.2:c.168-97_168-88del | NP_054787.2:n.168-97_168-88del | |
NM_014068.3:c.168-97_168-88del MANE Select | NP_054787.2:n.168-97_168-88del |