HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107701149A>G , CM000669.2:g.107701149A>G | GRCh38 |
NC_000007.13:g.107341594A>G , CM000669.1:g.107341594A>G | GRCh37 |
NC_000007.12:g.107128830A>G | NCBI36 |
NG_008489.1:g.45515A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.1756A>G MANE Select | ENSP00000494017.1:p.Arg586Gly | |
ENST00000644846.1:c.467A>G | ||
ENST00000265715.7:c.1756A>G | ENSP00000265715.3:p.Arg586Gly | |
ENST00000480841.5:n.605A>G | ||
ENST00000492030.2:n.91-678A>G | ||
NM_000441.1:c.1756A>G | NP_000432.1:p.Arg586Gly | |
XM_005250425.1:c.1756A>G | XP_005250482.1:p.Arg586Gly | |
XM_005250425.2:c.1756A>G | XP_005250482.1:p.Arg586Gly | |
XM_017012318.1:c.1678A>G | XP_016867807.1:p.Arg560Gly | |
NM_000441.2:c.1756A>G MANE Select | NP_000432.1:p.Arg586Gly |