HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101421883C>T , CM000671.2:g.101421883C>T | GRCh38 |
NC_000009.11:g.104184165C>T , CM000671.1:g.104184165C>T | GRCh37 |
NC_000009.10:g.103223986C>T | NCBI36 |
NG_012387.1:g.18898G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.1021G>A MANE Select | ENSP00000497767.1:p.Gly341Arg | |
ENST00000648064.1:c.1021G>A | ENSP00000497990.1:p.Gly341Arg | |
ENST00000648758.1:c.1021G>A | ENSP00000497731.1:p.Gly341Arg | |
ENST00000374855.8:c.1021G>A | ENSP00000363988.4:p.Gly341Arg | |
ENST00000616752.1:c.*33G>A | ENSP00000481363.1:n.*33G>A | |
NM_000035.3:c.1021G>A | NP_000026.2:p.Gly341Arg | |
NM_000035.4:c.1021G>A MANE Select | NP_000026.2:p.Gly341Arg |