HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73641339A= , CM000664.2:g.73641339A= | GRCh38 |
NC_000002.11:g.73868466A= , CM000664.1:g.73868466A= | GRCh37 |
NC_000002.10:g.73721974A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.290T= (NAT8) MANE Select | ENSP00000272425.3:p.Ile97= | |
ENST00000652439.1:n.243+14A= (ALMS1P1) | ||
ENST00000272425.3:c.290T= (NAT8) | ENSP00000272425.3:p.Ile97= | |
NM_003960.3:c.290T= (NAT8) | NP_003951.3:p.Ile97= | |
NM_003960.4:c.290T= (NAT8) MANE Select | NP_003951.3:p.Ile97= |