HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174621C>T , CM000674.2:g.21174621C>T | GRCh38 |
NC_000012.11:g.21327555C>T , CM000674.1:g.21327555C>T | GRCh37 |
NC_000012.10:g.21218822C>T | NCBI36 |
NG_011745.1:g.48428C>T , LRG_1022:g.48428C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.271C>T MANE Select | ENSP00000256958.2:p.Leu91= | |
ENST00000256958.2:c.271C>T | ENSP00000256958.2:p.Leu91= | |
ENST00000543498.5:c.426-2155C>T | ||
NM_006446.4:c.271C>T , LRG_1022t1:c.271C>T | NP_006437.3:p.Leu91= | |
NM_006446.5:c.271C>T MANE Select | NP_006437.3:p.Leu91= |