HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101425583G>C , CM000671.2:g.101425583G>C | GRCh38 |
NC_000009.11:g.104187865G>C , CM000671.1:g.104187865G>C | GRCh37 |
NC_000009.10:g.103227686G>C | NCBI36 |
NG_012387.1:g.15198C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.669C>G MANE Select | ENSP00000497767.1:p.Tyr223Ter | |
ENST00000648064.1:c.669C>G | ENSP00000497990.1:p.Tyr223Ter | |
ENST00000648758.1:c.669C>G | ENSP00000497731.1:p.Tyr223Ter | |
ENST00000649902.1:c.669C>G | ENSP00000497216.1:p.Tyr223Ter | |
ENST00000374855.8:c.669C>G | ENSP00000363988.4:p.Tyr223Ter | |
ENST00000468981.3:n.196C>G | ||
ENST00000616752.1:c.669C>G | ENSP00000481363.1:p.Tyr223Ter | |
NM_000035.3:c.669C>G | NP_000026.2:p.Tyr223Ter | |
NM_000035.4:c.669C>G MANE Select | NP_000026.2:p.Tyr223Ter |