HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50910015C>T , CM000676.2:g.50910015C>T | GRCh38 |
NC_000014.8:g.51376733C>T , CM000676.1:g.51376733C>T | GRCh37 |
NC_000014.7:g.50446483C>T | NCBI36 |
NG_012796.1:g.39516G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216392.8:c.2057G>A MANE Select | ENSP00000216392.7:p.Gly686Glu | |
ENST00000216392.7:c.2057G>A | ENSP00000216392.7:p.Gly686Glu | |
ENST00000532107.2:n.230G>A | ||
ENST00000532462.5:c.2057G>A | ENSP00000431657.1:p.Gly686Glu | |
ENST00000544180.6:c.1955G>A | ENSP00000443787.1:p.Gly652Glu | |
NM_001163940.1:c.1955G>A | NP_001157412.1:p.Gly652Glu | |
NM_002863.4:c.2057G>A | NP_002854.3:p.Gly686Glu | |
NM_002863.5:c.2057G>A MANE Select | NP_002854.3:p.Gly686Glu | |
NM_001163940.2:c.1955G>A | NP_001157412.1:p.Gly652Glu |