HGVS | Genome Assembly |
---|---|
NC_000001.11:g.197039222C>G , CM000663.2:g.197039222C>G | GRCh38 |
NC_000001.10:g.197008352C>G , CM000663.1:g.197008352C>G | GRCh37 |
NC_000001.9:g.195274975C>G | NCBI36 |
NG_012065.1:g.33046G>C , LRG_550:g.33046G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367412.2:c.*156G>C MANE Select | ENSP00000356382.2:n.*156G>C | |
ENST00000649282.1:c.897G>C | ENSP00000497116.1:n.897G>C | |
ENST00000367412.1:c.*156G>C | ENSP00000356382.1:n.*156G>C | |
NM_001994.2:c.*156G>C , LRG_550t1:c.*156G>C | NP_001985.2:n.*156G>C | |
XM_011509283.2:c.*1077G>C | XP_011507585.1:n.*1077G>C | |
XM_011509284.2:c.*1077G>C | XP_011507586.1:n.*1077G>C | |
XM_011509286.2:c.*1077G>C | XP_011507588.1:n.*1077G>C | |
NM_001994.3:c.*156G>C MANE Select | NP_001985.2:n.*156G>C |