HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48303957T>C , CM000675.2:g.48303957T>C | GRCh38 |
NC_000013.10:g.48878093T>C , CM000675.1:g.48878093T>C | GRCh37 |
NC_000013.9:g.47776094T>C | NCBI36 |
NG_009009.1:g.5211T>C , LRG_517:g.5211T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.45T>C MANE Select | ENSP00000267163.4:p.Ala15= | |
ENST00000646097.1:c.45T>C | ENSP00000496556.1:p.Ala15= | |
ENST00000650461.1:c.45T>C | ENSP00000497193.1:p.Ala15= | |
ENST00000267163.4:c.45T>C | ENSP00000267163.4:p.Ala15= | |
ENST00000467505.5:c.45T>C | ENSP00000434702.1:p.Ala15= | |
ENST00000525036.1:n.207T>C | ||
NM_000321.2:c.45T>C , LRG_517t1:c.45T>C | NP_000312.2:p.Ala15= | |
NM_000321.3:c.45T>C MANE Select | NP_000312.2:p.Ala15= |