HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2866978A>T , CM000686.2:g.2866978A>T | GRCh38 |
NC_000024.9:g.2735019A>T , CM000686.1:g.2735019A>T | GRCh37 |
NC_000024.8:g.2795019A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000250784.13:c.*84A>T MANE Select | ENSP00000250784.7:n.*84A>T | |
ENST00000250784.12:c.*84A>T | ENSP00000250784.7:n.*84A>T | |
ENST00000515575.1:n.42+12207A>T | ||
NM_001008.4:c.*84A>T MANE Select | NP_000999.1:n.*84A>T |