HGVS | Genome Assembly |
---|---|
NC_000002.12:g.31348833C= , CM000664.2:g.31348833C= | GRCh38 |
NC_000002.11:g.31571699C= , CM000664.1:g.31571699C= | GRCh37 |
NC_000002.10:g.31425203C= | NCBI36 |
NG_008871.1:g.70913G= | |
NG_008871.2:g.70913G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379416.4:c.3051+66G= MANE Select | ENSP00000368727.3:n.3051+66G= | |
ENST00000379416.3:c.3051+66G= | ENSP00000368727.3:n.3051+66G= | |
NM_000379.3:c.3051+66G= | NP_000370.2:n.3051+66G= | |
XM_011533095.1:c.3048+66G= | XP_011531397.1:n.3048+66G= | |
XM_011533096.1:c.3051+66G= | XP_011531398.1:n.3051+66G= | |
XM_011533095.2:c.3048+66G= | XP_011531397.1:n.3048+66G= | |
XM_011533096.2:c.3051+66G= | XP_011531398.1:n.3051+66G= | |
NM_000379.4:c.3051+66G= MANE Select | NP_000370.2:n.3051+66G= |