HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129061473del , CM000665.2:g.129061473del | GRCh38 |
NC_000003.11:g.128780316del , CM000665.1:g.128780316del | GRCh37 |
NC_000003.10:g.130263006del | NCBI36 |
NG_008715.1:g.5672del , LRG_477:g.5672del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307395.5:c.-138-21del MANE Select | ENSP00000303942.4:n.-138-21del | |
ENST00000307395.4:c.-138-21del | ENSP00000303942.4:n.-138-21del | |
NM_000174.4:c.-138-21del , LRG_477t1:c.-138-21del | NP_000165.1:n.-138-21del | |
XM_005247374.3:c.-138-21del | XP_005247431.1:n.-138-21del | |
XM_011512701.1:c.-138-21del | XP_011511003.1:n.-138-21del | |
XM_011512702.1:c.-12-255del | XP_011511004.1:n.-12-255del | |
NM_000174.5:c.-138-21del MANE Select | NP_000165.1:n.-138-21del |