HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50924101C>G , CM000676.2:g.50924101C>G | GRCh38 |
NC_000014.8:g.51390819C>G , CM000676.1:g.51390819C>G | GRCh37 |
NC_000014.7:g.50460569C>G | NCBI36 |
NG_012796.1:g.25430G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216392.8:c.529-1G>C MANE Select | ENSP00000216392.7:n.529-1G>C | |
ENST00000216392.7:c.529-1G>C | ENSP00000216392.7:n.529-1G>C | |
ENST00000530336.2:n.596-1G>C | ||
ENST00000532462.5:c.529-1G>C | ENSP00000431657.1:n.529-1G>C | |
ENST00000544180.6:c.427-1G>C | ENSP00000443787.1:n.427-1G>C | |
NM_001163940.1:c.427-1G>C | NP_001157412.1:n.427-1G>C | |
NM_002863.4:c.529-1G>C | NP_002854.3:n.529-1G>C | |
NM_002863.5:c.529-1G>C MANE Select | NP_002854.3:n.529-1G>C | |
NM_001163940.2:c.427-1G>C | NP_001157412.1:n.427-1G>C |