HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008221C= , CM000666.2:g.88008221C= | GRCh38 |
NC_000004.11:g.88929373C= , CM000666.1:g.88929373C= | GRCh37 |
NC_000004.10:g.89148397C= | NCBI36 |
NG_008604.1:g.5554C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.488C= MANE Select | ENSP00000237596.2:p.Pro163= | |
ENST00000237596.6:c.488C= | ENSP00000237596.2:p.Pro163= | |
NM_000297.3:c.488C= | NP_000288.1:p.Pro163= | |
XM_011532028.1:c.488C= | XP_011530330.1:p.Pro163= | |
XR_244632.2:n.583C= | ||
NR_156488.1:n.575C= | ||
XM_011532028.2:c.488C= | XP_011530330.1:p.Pro163= | |
NM_000297.4:c.488C= MANE Select | NP_000288.1:p.Pro163= | |
NR_156488.2:n.587C= |