HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951815T>C , CM000670.2:g.19951815T>C | GRCh38 |
NC_000008.10:g.19809326T>C , CM000670.1:g.19809326T>C | GRCh37 |
NC_000008.9:g.19853606T>C | NCBI36 |
NG_008855.1:g.17745T>C | |
NG_008855.2:g.55099T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.296T>C MANE Select | ENSP00000497642.1:p.Leu99Pro | |
ENST00000311322.8:c.296T>C | ENSP00000309757.6:p.Leu99Pro | |
ENST00000520959.5:c.68T>C | ENSP00000428496.1:p.Leu23Pro | |
ENST00000521994.1:n.553T>C | ||
ENST00000522701.5:c.296T>C | ENSP00000428557.1:p.Leu99Pro | |
ENST00000524029.5:c.296T>C | ENSP00000428237.1:p.Leu99Pro | |
NM_000237.2:c.296T>C | NP_000228.1:p.Leu99Pro | |
NM_000237.3:c.296T>C MANE Select | NP_000228.1:p.Leu99Pro |