HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274700_2274833del , CM000681.2:g.2274700_2274833del | GRCh38 |
NC_000019.9:g.2274699_2274832del , CM000681.1:g.2274699_2274832del | GRCh37 |
NC_000019.8:g.2225699_2225832del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*857_*990del MANE Select | ENSP00000345102.3:n.*857_*990del | |
ENST00000342063.4:c.*857_*990del | ENSP00000345102.3:n.*857_*990del | |
ENST00000621615.1:c.146+4956_146+5089del | ENSP00000481965.1:n.146+4956_146+5089del | |
NM_198532.2:c.*857_*990del | NP_940934.1:n.*857_*990del | |
NM_198532.3:c.*857_*990del MANE Select | NP_940934.1:n.*857_*990del |