HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174633A= , CM000674.2:g.21174633A= | GRCh38 |
NC_000012.11:g.21327567A= , CM000674.1:g.21327567A= | GRCh37 |
NC_000012.10:g.21218834A= | NCBI36 |
NG_011745.1:g.48440A= , LRG_1022:g.48440A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.283A= MANE Select | ENSP00000256958.2:p.Lys95= | |
ENST00000256958.2:c.283A= | ENSP00000256958.2:p.Lys95= | |
ENST00000543498.5:c.426-2143A= | ||
NM_006446.4:c.283A= , LRG_1022t1:c.283A= | NP_006437.3:p.Lys95= | |
NM_006446.5:c.283A= MANE Select | NP_006437.3:p.Lys95= |