HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31580724A>G , CM000664.2:g.31580724A>G | GRCh38 |
NC_000002.11:g.31805794A>G , CM000664.1:g.31805794A>G | GRCh37 |
NC_000002.10:g.31659298A>G | NCBI36 |
NG_008365.1:g.5248T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622030.2:c.177T>C MANE Select | ENSP00000477587.1:p.Pro59= | |
ENST00000622030.1:c.177T>C | ENSP00000477587.1:p.Pro59= | |
NM_000348.3:c.177T>C | NP_000339.2:p.Pro59= | |
XM_011533068.1:c.177T>C | XP_011531370.1:p.Pro59= | |
XM_011533070.1:c.27-46958T>C | XP_011531372.1:n.27-46958T>C | |
XM_011533071.1:c.27-46958T>C | XP_011531373.1:n.27-46958T>C | |
XM_011533072.1:c.27-46958T>C | XP_011531374.1:n.27-46958T>C | |
XM_011533072.2:c.27-46958T>C | XP_011531374.1:n.27-46958T>C | |
NM_000348.4:c.177T>C MANE Select | NP_000339.2:p.Pro59= |