HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110582075G>C , CM000672.2:g.110582075G>C | GRCh38 |
NC_000010.10:g.112341833G>C , CM000672.1:g.112341833G>C | GRCh37 |
NC_000010.9:g.112331823G>C | NCBI36 |
NG_012217.1:g.19385G>C , LRG_774:g.19385G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.833G>C | ||
ENST00000687823.1:n.614G>C | ||
ENST00000689932.1:n.2763G>C | ||
ENST00000691297.1:n.833G>C | ||
ENST00000691527.1:n.1503G>C | ||
ENST00000692792.1:n.819G>C | ||
ENST00000361804.5:c.700G>C MANE Select | ENSP00000354720.5:p.Glu234Gln | |
ENST00000361804.4:c.700G>C | ENSP00000354720.4:p.Glu234Gln | |
NM_005445.3:c.700G>C , LRG_774t1:c.700G>C | NP_005436.1:p.Glu234Gln | |
NM_005445.4:c.700G>C MANE Select | NP_005436.1:p.Glu234Gln |