HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110601688A>C , CM000672.2:g.110601688A>C | GRCh38 |
NC_000010.10:g.112361446A>C , CM000672.1:g.112361446A>C | GRCh37 |
NC_000010.9:g.112351436A>C | NCBI36 |
NG_012217.1:g.38998A>C , LRG_774:g.38998A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.4929A>C | ||
ENST00000685743.1:n.2404A>C | ||
ENST00000686057.1:n.1047A>C | ||
ENST00000689321.1:n.1659A>C | ||
ENST00000689986.1:n.485A>C | ||
ENST00000361804.5:c.2696A>C MANE Select | ENSP00000354720.5:p.Lys899Thr | |
ENST00000361804.4:c.2696A>C | ENSP00000354720.4:p.Lys899Thr | |
NM_005445.3:c.2696A>C , LRG_774t1:c.2696A>C | NP_005436.1:p.Lys899Thr | |
NM_005445.4:c.2696A>C MANE Select | NP_005436.1:p.Lys899Thr |