HGVS | Genome Assembly |
---|---|
NC_000023.11:g.634554G>T , CM000685.2:g.634554G>T | GRCh38 |
NC_000023.10:g.595289G>T , CM000685.1:g.595289G>T | GRCh37 |
NC_000023.9:g.515289G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000686671.1:c.278-64G>T MANE Select | ENSP00000508521.1:n.278-64G>T | |
ENST00000334060.8:c.278-64G>T | ENSP00000335505.3:n.278-64G>T | |
ENST00000381575.6:c.278-64G>T | ENSP00000370987.1:n.278-64G>T | |
ENST00000381578.6:c.278-64G>T | ENSP00000370990.1:n.278-64G>T | |
ENST00000554971.6:c.278-64G>T | ENSP00000452016.1:n.278-64G>T |