HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74917221T= , CM000679.2:g.74917221T= | GRCh38 |
NC_000017.10:g.72913315T= , CM000679.1:g.72913315T= | GRCh37 |
NC_000017.9:g.70424910T= | NCBI36 |
NG_007882.1:g.11037A= | |
NG_007882.2:g.11043A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.*852A= MANE Select | ENSP00000480279.1:n.*852A= | |
ENST00000614341.4:c.*852A= | ENSP00000480279.1:n.*852A= | |
NM_001282489.2:c.*852A= | NP_001269418.1:n.*852A= | |
NM_173477.4:c.*852A= | NP_775748.2:n.*852A= | |
XM_011524296.1:c.*852A= | XP_011522598.1:n.*852A= | |
XM_011524296.2:c.*852A= | XP_011522598.1:n.*852A= | |
NM_173477.5:c.*852A= MANE Select | NP_775748.2:n.*852A= | |
NM_001282489.3:c.*852A= | NP_001269418.1:n.*852A= |