HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75008951C>G , CM000676.2:g.75008951C>G | GRCh38 |
NC_000014.8:g.75475654C>G , CM000676.1:g.75475654C>G | GRCh37 |
NC_000014.7:g.74545407C>G | NCBI36 |
NG_013333.1:g.11043C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.899-80C>G MANE Select | ENSP00000266126.5:n.899-80C>G | |
ENST00000266126.9:c.899-80C>G | ENSP00000266126.5:n.899-80C>G | |
ENST00000556668.1:n.479-80C>G | ||
NM_014239.3:c.899-80C>G | NP_055054.1:n.899-80C>G | |
NM_014239.4:c.899-80C>G MANE Select | NP_055054.1:n.899-80C>G |