HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31526187T= , CM000664.2:g.31526187T= | GRCh38 |
NC_000002.11:g.31751257T= , CM000664.1:g.31751257T= | GRCh37 |
NC_000002.10:g.31604761T= | NCBI36 |
NG_008365.1:g.59785A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622030.2:c.*9A= MANE Select | ENSP00000477587.1:n.*9A= | |
ENST00000622030.1:c.*9A= | ENSP00000477587.1:n.*9A= | |
NM_000348.3:c.*9A= | NP_000339.2:n.*9A= | |
XM_011533069.1:c.*9A= | XP_011531371.1:n.*9A= | |
XM_011533070.1:c.*9A= | XP_011531372.1:n.*9A= | |
XM_011533071.1:c.*9A= | XP_011531373.1:n.*9A= | |
XM_011533072.1:c.*9A= | XP_011531374.1:n.*9A= | |
XM_011533069.2:c.*9A= | XP_011531371.1:n.*9A= | |
XM_011533072.2:c.*9A= | XP_011531374.1:n.*9A= | |
NM_000348.4:c.*9A= MANE Select | NP_000339.2:n.*9A= |