HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7527789_7527790insCCAGCT , CM000681.2:g.7527789_7527790insCCAGCT | GRCh38 |
NC_000019.9:g.7592675_7592676insCCAGCT , CM000681.1:g.7592675_7592676insCCAGCT | GRCh37 |
NC_000019.8:g.7498675_7498676insCCAGCT | NCBI36 |
NG_015806.1:g.10180_10181insCCAGCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.681-75_681-74insCCAGCT MANE Select | ENSP00000264079.5:n.681-75_681-74insCCAGC... | |
ENST00000264079.10:c.681-75_681-74insCCAGCT | ENSP00000264079.5:n.681-75_681-74insCCAGC... | |
ENST00000394321.9:n.921_922insCCAGCT | ||
ENST00000601003.1:c.572-75_572-74insCCAGCT | ENSP00000469074.1:n.572-75_572-74insCCAGC... | |
NM_020533.2:c.681-75_681-74insCCAGCT | NP_065394.1:n.681-75_681-74insCCAGCT | |
NM_020533.3:c.681-75_681-74insCCAGCT MANE Select | NP_065394.1:n.681-75_681-74insCCAGCT |