HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274953_2274959dup , CM000681.2:g.2274953_2274959dup | GRCh38 |
NC_000019.9:g.2274952_2274958dup , CM000681.1:g.2274952_2274958dup | GRCh37 |
NC_000019.8:g.2225952_2225958dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*726_*732dup MANE Select | ENSP00000345102.3:n.*726_*732dup | |
ENST00000342063.4:c.*726_*732dup | ENSP00000345102.3:n.*726_*732dup | |
ENST00000621615.1:c.146+5209_146+5215dup | ENSP00000481965.1:n.146+5209_146+5215dup | |
NM_198532.2:c.*726_*732dup | NP_940934.1:n.*726_*732dup | |
NM_198532.3:c.*726_*732dup MANE Select | NP_940934.1:n.*726_*732dup |