HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111539C>G , CM000670.2:g.118111539C>G | GRCh38 |
NC_000008.10:g.119123778C>G , CM000670.1:g.119123778C>G | GRCh37 |
NC_000008.9:g.119192959C>G | NCBI36 |
NG_007455.2:g.5281G>C , LRG_493:g.5281G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-493G>C MANE Select | ENSP00000367446.3:n.-493G>C | |
ENST00000378204.6:c.-493G>C | ENSP00000367446.2:n.-493G>C | |
NM_000127.2:c.-493G>C , LRG_493t1:c.-493G>C | NP_000118.2:n.-493G>C | |
NM_000127.3:c.-493G>C MANE Select | NP_000118.2:n.-493G>C |