HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2275069_2275102del , CM000681.2:g.2275069_2275102del | GRCh38 |
NC_000019.9:g.2275068_2275101del , CM000681.1:g.2275068_2275101del | GRCh37 |
NC_000019.8:g.2226068_2226101del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000342063.5:c.*581_*614del MANE Select | ENSP00000345102.3:n.*581_*614del | |
ENST00000342063.4:c.*581_*614del | ENSP00000345102.3:n.*581_*614del | |
ENST00000621615.1:c.146+5325_146+5358del | ENSP00000481965.1:n.146+5325_146+5358del | |
NM_198532.2:c.*581_*614del | NP_940934.1:n.*581_*614del | |
NM_198532.3:c.*581_*614del MANE Select | NP_940934.1:n.*581_*614del |