HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38401342G>C , CM000685.2:g.38401342G>C | GRCh38 |
NC_000023.10:g.38260595G>C , CM000685.1:g.38260595G>C | GRCh37 |
NC_000023.9:g.38145539G>C | NCBI36 |
NG_008471.1:g.53860G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.454G>C MANE Select | ENSP00000039007.4:p.Ala152Pro | |
ENST00000643344.1:c.*204G>C | ENSP00000496606.1:n.*204G>C | |
ENST00000039007.4:c.454G>C | ENSP00000039007.4:p.Ala152Pro | |
ENST00000465127.1:c.172-264779G>C | ENSP00000417050.1:n.172-264779G>C | |
ENST00000488812.1:n.491G>C | ||
NM_000531.5:c.454G>C | NP_000522.3:p.Ala152Pro | |
XM_017029556.1:c.454G>C | XP_016885045.1:p.Ala152Pro | |
NM_000531.6:c.454G>C MANE Select | NP_000522.3:p.Ala152Pro |