HGVS | Genome Assembly |
---|---|
NC_000023.11:g.634560C= , CM000685.2:g.634560C= | GRCh38 |
NC_000023.10:g.595295C= , CM000685.1:g.595295C= | GRCh37 |
NC_000023.9:g.515295C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000686671.1:c.278-58C= MANE Select | ENSP00000508521.1:n.278-58C= | |
ENST00000334060.8:c.278-58C= | ENSP00000335505.3:n.278-58C= | |
ENST00000381575.6:c.278-58C= | ENSP00000370987.1:n.278-58C= | |
ENST00000381578.6:c.278-58C= | ENSP00000370990.1:n.278-58C= | |
ENST00000554971.6:c.278-58C= | ENSP00000452016.1:n.278-58C= |