HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775434T>C , CM000672.2:g.94775434T>C | GRCh38 |
NC_000010.10:g.96535191T>C , CM000672.1:g.96535191T>C | GRCh37 |
NC_000010.9:g.96525181T>C | NCBI36 |
NG_008384.2:g.17729T>C | |
NG_008384.3:g.17754T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.376T>C MANE Select | ENSP00000360372.3:p.Phe126Leu | |
ENST00000645461.1:n.1429T>C | ||
ENST00000371321.7:c.376T>C | ENSP00000360372.3:p.Phe126Leu | |
ENST00000464755.1:c.1139T>C | ENSP00000483243.1:n.1139T>C | |
ENST00000480405.2:c.376T>C | ENSP00000483847.1:p.Phe126Leu | |
NM_000769.2:c.376T>C | NP_000760.1:p.Phe126Leu | |
NM_000769.4:c.376T>C MANE Select | NP_000760.1:p.Phe126Leu |