HGVS | Genome Assembly |
---|---|
NC_000003.12:g.87259798_87259800del , CM000665.2:g.87259798_87259800del | GRCh38 |
NC_000003.11:g.87308948_87308950del , CM000665.1:g.87308948_87308950del | GRCh37 |
NC_000003.10:g.87391638_87391640del | NCBI36 |
NG_008225.2:g.21789_21791del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344265.8:c.*95_*97del | ENSP00000342931.3:n.*95_*97del | |
ENST00000350375.7:c.*95_*97del MANE Select | ENSP00000263781.2:n.*95_*97del | |
ENST00000344265.7:c.*95_*97del | ENSP00000342931.3:n.*95_*97del | |
ENST00000350375.6:c.*95_*97del | ENSP00000263781.2:n.*95_*97del | |
NM_000306.3:c.*95_*97del | NP_000297.1:n.*95_*97del | |
NM_001122757.2:c.*95_*97del | NP_001116229.1:n.*95_*97del | |
NM_000306.4:c.*95_*97del MANE Select | NP_000297.1:n.*95_*97del | |
NM_001122757.3:c.*95_*97del | NP_001116229.1:n.*95_*97del |