HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110575344T>C , CM000672.2:g.110575344T>C | GRCh38 |
NC_000010.10:g.112335102T>C , CM000672.1:g.112335102T>C | GRCh37 |
NC_000010.9:g.112325092T>C | NCBI36 |
NG_012217.1:g.12654T>C , LRG_774:g.12654T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684988.1:n.272T>C | ||
ENST00000687823.1:n.53T>C | ||
ENST00000689932.1:n.2202T>C | ||
ENST00000691297.1:n.272T>C | ||
ENST00000691527.1:n.229T>C | ||
ENST00000692792.1:n.258T>C | ||
ENST00000361804.5:c.139T>C MANE Select | ENSP00000354720.5:p.Phe47Leu | |
ENST00000361804.4:c.139T>C | ENSP00000354720.4:p.Phe47Leu | |
ENST00000462899.1:n.285T>C | ||
NM_005445.3:c.139T>C , LRG_774t1:c.139T>C | NP_005436.1:p.Phe47Leu | |
NM_005445.4:c.139T>C MANE Select | NP_005436.1:p.Phe47Leu |