HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951821A>T , CM000670.2:g.19951821A>T | GRCh38 |
NC_000008.10:g.19809332A>T , CM000670.1:g.19809332A>T | GRCh37 |
NC_000008.9:g.19853612A>T | NCBI36 |
NG_008855.1:g.17751A>T | |
NG_008855.2:g.55105A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.302A>T MANE Select | ENSP00000497642.1:p.Lys101Met | |
ENST00000311322.8:c.302A>T | ENSP00000309757.6:p.Lys101Met | |
ENST00000520959.5:c.74A>T | ENSP00000428496.1:p.Lys25Met | |
ENST00000521994.1:n.559A>T | ||
ENST00000522701.5:c.302A>T | ENSP00000428557.1:p.Lys101Met | |
ENST00000524029.5:c.302A>T | ENSP00000428237.1:p.Lys101Met | |
NM_000237.2:c.302A>T | NP_000228.1:p.Lys101Met | |
NM_000237.3:c.302A>T MANE Select | NP_000228.1:p.Lys101Met |