HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101425498C= , CM000671.2:g.101425498C= | GRCh38 |
NC_000009.11:g.104187780C= , CM000671.1:g.104187780C= | GRCh37 |
NC_000009.10:g.103227601C= | NCBI36 |
NG_012387.1:g.15283G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647789.2:c.754G= MANE Select | ENSP00000497767.1:p.Ala252= | |
ENST00000648064.1:c.754G= | ENSP00000497990.1:p.Ala252= | |
ENST00000648758.1:c.754G= | ENSP00000497731.1:p.Ala252= | |
ENST00000649902.1:c.754G= | ENSP00000497216.1:p.Ala252= | |
ENST00000374855.8:c.754G= | ENSP00000363988.4:p.Ala252= | |
ENST00000616752.1:c.754G= | ENSP00000481363.1:p.Ala252= | |
NM_000035.3:c.754G= | NP_000026.2:p.Ala252= | |
NM_000035.4:c.754G= MANE Select | NP_000026.2:p.Ala252= |