HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147132246G>C , CM000669.2:g.147132246G>C | GRCh38 |
NC_000007.13:g.146829338G>C , CM000669.1:g.146829338G>C | GRCh37 |
NC_000007.12:g.146460271G>C | NCBI36 |
NG_007092.2:g.1020886G>C | |
NG_007092.3:g.1021246G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1085G>C MANE Select | ENSP00000354778.3:p.Gly362Ala | |
ENST00000636561.1:n.988G>C | ||
ENST00000636870.1:n.947G>C | ||
ENST00000637150.1:n.1014G>C | ||
ENST00000637694.1:n.988G>C | ||
ENST00000637825.1:n.568G>C | ||
ENST00000638117.1:n.988G>C | ||
ENST00000361727.7:c.1085G>C | ENSP00000354778.3:p.Gly362Ala | |
NM_014141.5:c.1085G>C | NP_054860.1:p.Gly362Ala | |
XM_017011950.2:c.1085G>C | XP_016867439.1:p.Gly362Ala | |
NM_014141.6:c.1085G>C MANE Select | NP_054860.1:p.Gly362Ala |