HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31580899A= , CM000664.2:g.31580899A= | GRCh38 |
NC_000002.11:g.31805968A= , CM000664.1:g.31805968A= | GRCh37 |
NC_000002.10:g.31659472A= | NCBI36 |
NG_008365.1:g.5073T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000622030.2:c.2T= MANE Select | ENSP00000477587.1:p.Met1= | |
ENST00000622030.1:c.2T= | ENSP00000477587.1:p.Met1= | |
NM_000348.3:c.2T= | NP_000339.2:p.Met1= | |
XM_011533068.1:c.2T= | XP_011531370.1:p.Met1= | |
XM_011533070.1:c.27-47133T= | XP_011531372.1:n.27-47133T= | |
XM_011533071.1:c.27-47133T= | XP_011531373.1:n.27-47133T= | |
XM_011533072.1:c.27-47133T= | XP_011531374.1:n.27-47133T= | |
XM_011533072.2:c.27-47133T= | XP_011531374.1:n.27-47133T= | |
NM_000348.4:c.2T= MANE Select | NP_000339.2:p.Met1= |