HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312655G>C , CM000673.2:g.118312655G>C | GRCh38 |
NC_000011.9:g.118183370G>C , CM000673.1:g.118183370G>C | GRCh37 |
NC_000011.8:g.117688580G>C | NCBI36 |
NG_007383.1:g.13076G>C , LRG_38:g.13076G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.141G>C MANE Select | ENSP00000354566.4:p.Leu47Phe | |
ENST00000361763.8:c.141G>C | ENSP00000354566.4:p.Leu47Phe | |
ENST00000526146.5:n.687G>C | ||
ENST00000528435.5:n.694G>C | ||
ENST00000528600.1:c.123G>C | ENSP00000433975.1:p.Leu41Phe | |
ENST00000529713.5:n.247G>C | ||
ENST00000531913.1:n.512G>C | ||
NM_000733.3:c.141G>C , LRG_38t1:c.141G>C | NP_000724.1:p.Leu47Phe | |
NM_000733.4:c.141G>C MANE Select | NP_000724.1:p.Leu47Phe |