HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739645_86739647del , CM000670.2:g.86739645_86739647del | GRCh38 |
NC_000008.10:g.87751873_87751875del , CM000670.1:g.87751873_87751875del | GRCh37 |
NC_000008.9:g.87820989_87820991del | NCBI36 |
NG_016980.1:g.9029_9031del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.211+8_211+10del MANE Select | ENSP00000316605.5:n.211+8_211+10del | |
ENST00000681746.1:c.211+8_211+10del | ENSP00000505959.1:n.211+8_211+10del | |
ENST00000320005.5:c.211+8_211+10del | ENSP00000316605.5:n.211+8_211+10del | |
ENST00000519777.1:n.193+8_193+10del | ||
NM_019098.4:c.211+8_211+10del | NP_061971.3:n.211+8_211+10del | |
NM_019098.5:c.211+8_211+10del MANE Select | NP_061971.3:n.211+8_211+10del |