HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24278558A>G , CM000668.2:g.24278558A>G | GRCh38 |
NC_000006.11:g.24278786A>G , CM000668.1:g.24278786A>G | GRCh37 |
NC_000006.10:g.24386765A>G | NCBI36 |
NG_012829.1:g.84495T>C | |
NG_012829.2:g.109735T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.760-347T>C MANE Select | ENSP00000367715.3:n.760-347T>C | |
ENST00000378454.7:c.760-347T>C | ENSP00000367715.3:n.760-347T>C | |
NM_001195610.1:c.760-347T>C | NP_001182539.1:n.760-347T>C | |
NM_016356.4:c.760-347T>C | NP_057440.2:n.760-347T>C | |
NM_016356.5:c.760-347T>C MANE Select | NP_057440.2:n.760-347T>C | |
NM_001195610.2:c.760-347T>C | NP_001182539.1:n.760-347T>C |