HGVS | Genome Assembly |
---|---|
NC_000008.11:g.81478651A>C , CM000670.2:g.81478651A>C | GRCh38 |
NC_000008.10:g.82390886A>C , CM000670.1:g.82390886A>C | GRCh37 |
NC_000008.9:g.82553441A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256104.5:c.*214T>G MANE Select | ENSP00000256104.4:n.*214T>G | |
ENST00000256104.4:c.*214T>G | ENSP00000256104.4:n.*214T>G | |
NM_001442.2:c.*214T>G | NP_001433.1:n.*214T>G | |
XR_001745980.1:n.514+16677A>C | ||
NM_001442.3:c.*214T>G MANE Select | NP_001433.1:n.*214T>G |