HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75009090C>A , CM000676.2:g.75009090C>A | GRCh38 |
NC_000014.8:g.75475793C>A , CM000676.1:g.75475793C>A | GRCh37 |
NC_000014.7:g.74545546C>A | NCBI36 |
NG_013333.1:g.11182C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.958C>A MANE Select | ENSP00000266126.5:p.Leu320Ile | |
ENST00000266126.9:c.958C>A | ENSP00000266126.5:p.Leu320Ile | |
ENST00000556668.1:n.538C>A | ||
NM_014239.3:c.958C>A | NP_055054.1:p.Leu320Ile | |
NM_014239.4:c.958C>A MANE Select | NP_055054.1:p.Leu320Ile |