HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215701T>C , CM000674.2:g.21215701T>C | GRCh38 |
NC_000012.11:g.21368635T>C , CM000674.1:g.21368635T>C | GRCh37 |
NC_000012.10:g.21259902T>C | NCBI36 |
NG_011745.1:g.89508T>C , LRG_1022:g.89508T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1418T>C MANE Select | ENSP00000256958.2:n.1498-1418T>C | |
ENST00000256958.2:c.1498-1418T>C | ENSP00000256958.2:n.1498-1418T>C | |
NM_006446.4:c.1498-1418T>C , LRG_1022t1:c.1498-1418T>C | NP_006437.3:n.1498-1418T>C | |
NM_006446.5:c.1498-1418T>C MANE Select | NP_006437.3:n.1498-1418T>C |