HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7526519G>A , CM000681.2:g.7526519G>A | GRCh38 |
NC_000019.9:g.7591405G>A , CM000681.1:g.7591405G>A | GRCh37 |
NC_000019.8:g.7497405G>A | NCBI36 |
NG_015806.1:g.8910G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.318G>A MANE Select | ENSP00000264079.5:p.Leu106= | |
ENST00000264079.10:c.318G>A | ENSP00000264079.5:p.Leu106= | |
ENST00000394321.9:n.398G>A | ||
ENST00000596008.1:n.280G>A | ||
ENST00000598406.1:n.139G>A | ||
ENST00000601003.1:c.318G>A | ENSP00000469074.1:p.Leu106= | |
NM_020533.2:c.318G>A | NP_065394.1:p.Leu106= | |
NM_020533.3:c.318G>A MANE Select | NP_065394.1:p.Leu106= |