HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110914201C>G , CM000674.2:g.110914201C>G | GRCh38 |
NC_000012.11:g.111352005C>G , CM000674.1:g.111352005C>G | GRCh37 |
NC_000012.10:g.109836388C>G | NCBI36 |
NG_007554.1:g.11377G>C , LRG_393:g.11377G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.259G>C MANE Select | ENSP00000228841.8:p.Gly87Arg | |
ENST00000663220.1:c.202G>C | ENSP00000499568.1:p.Gly68Arg | |
ENST00000228841.12:c.259G>C | ENSP00000228841.7:p.Gly87Arg | |
ENST00000548438.1:c.217G>C | ENSP00000447154.1:p.Gly73Arg | |
ENST00000549029.1:n.90G>C | ||
NM_000432.3:c.259G>C , LRG_393t1:c.259G>C | NP_000423.2:p.Gly87Arg | |
NM_000432.4:c.259G>C MANE Select | NP_000423.2:p.Gly87Arg |