HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174647C= , CM000674.2:g.21174647C= | GRCh38 |
NC_000012.11:g.21327581C= , CM000674.1:g.21327581C= | GRCh37 |
NC_000012.10:g.21218848C= | NCBI36 |
NG_011745.1:g.48454C= , LRG_1022:g.48454C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.297C= MANE Select | ENSP00000256958.2:p.Ile99= | |
ENST00000256958.2:c.297C= | ENSP00000256958.2:p.Ile99= | |
ENST00000543498.5:c.426-2129C= | ||
NM_006446.4:c.297C= , LRG_1022t1:c.297C= | NP_006437.3:p.Ile99= | |
NM_006446.5:c.297C= MANE Select | NP_006437.3:p.Ile99= |