HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780564T>C , CM000672.2:g.94780564T>C | GRCh38 |
NC_000010.10:g.96540321T>C , CM000672.1:g.96540321T>C | GRCh37 |
NC_000010.9:g.96530311T>C | NCBI36 |
NG_008384.2:g.22859T>C | |
NG_008384.3:g.22884T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.547T>C MANE Select | ENSP00000360372.3:p.Phe183Leu | |
ENST00000645461.1:n.1600T>C | ||
ENST00000371321.7:c.547T>C | ENSP00000360372.3:p.Phe183Leu | |
ENST00000464755.1:c.1310T>C | ENSP00000483243.1:n.1310T>C | |
NM_000769.2:c.547T>C | NP_000760.1:p.Phe183Leu | |
NM_000769.4:c.547T>C MANE Select | NP_000760.1:p.Phe183Leu |