HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34256438_34256440del , CM000679.2:g.34256438_34256440del | GRCh38 |
NC_000017.10:g.32583457_32583459del , CM000679.1:g.32583457_32583459del | GRCh37 |
NC_000017.9:g.29607570_29607572del | NCBI36 |
NG_012123.1:g.6162_6164del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000580907.6:c.*95_*97del | ENSP00000462156.1:n.*95_*97del | |
ENST00000624362.2:n.1154_1156del | ||
ENST00000225831.4:c.194+99_194+101del MANE Select | ENSP00000225831.4:n.194+99_194+101del | |
ENST00000580907.5:c.*95_*97del | ENSP00000462156.1:n.*95_*97del | |
ENST00000582017.1:n.231_233del | ||
NM_002982.3:c.194+99_194+101del | NP_002973.1:n.194+99_194+101del | |
NM_002982.4:c.194+99_194+101del MANE Select | NP_002973.1:n.194+99_194+101del |