HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625387C>A , CM000673.2:g.22625387C>A | GRCh38 |
NC_000011.9:g.22646933C>A , CM000673.1:g.22646933C>A | GRCh37 |
NC_000011.8:g.22603509C>A | NCBI36 |
NG_007425.1:g.5455G>T , LRG_527:g.5455G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327470.6:c.424G>T MANE Select | ENSP00000330875.3:p.Ala142Ser | |
ENST00000327470.4:c.424G>T | ENSP00000330875.3:p.Ala142Ser | |
NM_022725.3:c.424G>T , LRG_527t1:c.424G>T | NP_073562.1:p.Ala142Ser | |
NM_022725.4:c.424G>T MANE Select | NP_073562.1:p.Ala142Ser |