HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107701141A>C , CM000669.2:g.107701141A>C | GRCh38 |
NC_000007.13:g.107341586A>C , CM000669.1:g.107341586A>C | GRCh37 |
NC_000007.12:g.107128822A>C | NCBI36 |
NG_008489.1:g.45507A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.1748A>C MANE Select | ENSP00000494017.1:p.Lys583Thr | |
ENST00000644846.1:c.459A>C | ||
ENST00000265715.7:c.1748A>C | ENSP00000265715.3:p.Lys583Thr | |
ENST00000480841.5:n.597A>C | ||
ENST00000492030.2:n.91-686A>C | ||
NM_000441.1:c.1748A>C | NP_000432.1:p.Lys583Thr | |
XM_005250425.1:c.1748A>C | XP_005250482.1:p.Lys583Thr | |
XM_005250425.2:c.1748A>C | XP_005250482.1:p.Lys583Thr | |
XM_017012318.1:c.1670A>C | XP_016867807.1:p.Lys557Thr | |
NM_000441.2:c.1748A>C MANE Select | NP_000432.1:p.Lys583Thr |