HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101428478T>A , CM000671.2:g.101428478T>A | GRCh38 |
NC_000009.11:g.104190760T>A , CM000671.1:g.104190760T>A | GRCh37 |
NC_000009.10:g.103230581T>A | NCBI36 |
NG_012387.1:g.12303A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.370A>T MANE Select | ENSP00000497767.1:p.Thr124Ser | |
ENST00000648064.1:c.370A>T | ENSP00000497990.1:p.Thr124Ser | |
ENST00000648758.1:c.370A>T | ENSP00000497731.1:p.Thr124Ser | |
ENST00000649902.1:c.370A>T | ENSP00000497216.1:p.Thr124Ser | |
ENST00000374855.8:c.370A>T | ENSP00000363988.4:p.Thr124Ser | |
ENST00000468981.3:n.67+1331A>T | ||
ENST00000616752.1:c.370A>T | ENSP00000481363.1:p.Thr124Ser | |
NM_000035.3:c.370A>T | NP_000026.2:p.Thr124Ser | |
NM_000035.4:c.370A>T MANE Select | NP_000026.2:p.Thr124Ser |