HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64604735C>A , CM000670.2:g.64604735C>A | GRCh38 |
NC_000008.10:g.65517292C>A , CM000670.1:g.65517292C>A | GRCh37 |
NC_000008.9:g.65679846C>A | NCBI36 |
NG_008338.1:g.199057G>T | |
NG_008338.2:g.199057G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000310193.4:c.1180G>T MANE Select | ENSP00000310721.3:p.Ala394Ser | |
ENST00000310193.3:c.1180G>T | ENSP00000310721.3:p.Ala394Ser | |
ENST00000523954.1:n.454G>T | ||
NM_004820.3:c.1180G>T | NP_004811.1:p.Ala394Ser | |
NM_001324112.1:c.1180G>T | NP_001311041.1:p.Ala394Ser | |
NM_004820.4:c.1180G>T | NP_004811.1:p.Ala394Ser | |
XM_017014002.1:c.1246G>T | XP_016869491.1:p.Ala416Ser | |
NM_004820.5:c.1180G>T MANE Select | NP_004811.1:p.Ala394Ser | |
NM_001324112.2:c.1180G>T | NP_001311041.1:p.Ala394Ser |