HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110573724G>C , CM000672.2:g.110573724G>C | GRCh38 |
NC_000010.10:g.112333482G>C , CM000672.1:g.112333482G>C | GRCh37 |
NC_000010.9:g.112323472G>C | NCBI36 |
NG_012217.1:g.11034G>C , LRG_774:g.11034G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.242G>C | ||
ENST00000687823.1:n.45-1612G>C | ||
ENST00000689932.1:n.582G>C | ||
ENST00000691297.1:n.242G>C | ||
ENST00000691527.1:n.199G>C | ||
ENST00000692792.1:n.228G>C | ||
ENST00000361804.5:c.109G>C MANE Select | ENSP00000354720.5:p.Gly37Arg | |
ENST00000361804.4:c.109G>C | ENSP00000354720.4:p.Gly37Arg | |
ENST00000462899.1:n.255G>C | ||
NM_005445.3:c.109G>C , LRG_774t1:c.109G>C | NP_005436.1:p.Gly37Arg | |
NM_005445.4:c.109G>C MANE Select | NP_005436.1:p.Gly37Arg |