HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1411154del , CM000667.2:g.1411154del | GRCh38 |
NC_000005.9:g.1411269del , CM000667.1:g.1411269del | GRCh37 |
NC_000005.8:g.1464269del | NCBI36 |
NG_015885.1:g.39277del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1269+91del MANE Select | ENSP00000270349.9:n.1269+91del | |
ENST00000270349.11:c.1269+91del | ENSP00000270349.9:n.1269+91del | |
NM_001044.4:c.1269+91del | NP_001035.1:n.1269+91del | |
NM_001044.5:c.1269+91del MANE Select | NP_001035.1:n.1269+91del |