HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218893170C>G , CM000664.2:g.218893170C>G | GRCh38 |
NC_000002.11:g.219757892C>G , CM000664.1:g.219757892C>G | GRCh37 |
NC_000002.10:g.219466136C>G | NCBI36 |
NG_012179.1:g.17638C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000258411.8:c.1153C>G MANE Select | ENSP00000258411.3:p.Arg385Gly | |
ENST00000258411.7:c.1153C>G | ENSP00000258411.3:p.Arg385Gly | |
NM_025216.2:c.1153C>G | NP_079492.2:p.Arg385Gly | |
XM_011511928.1:c.1102C>G | XP_011510230.1:p.Arg368Gly | |
XM_011511929.1:c.1057C>G | XP_011510231.1:p.Arg353Gly | |
XM_011511930.1:c.773C>G | XP_011510232.1:p.Ala258Gly | |
XM_011511929.2:c.1057C>G | XP_011510231.1:p.Arg353Gly | |
NM_025216.3:c.1153C>G MANE Select | NP_079492.2:p.Arg385Gly |