HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94988925A>C , CM000672.2:g.94988925A>C | GRCh38 |
NC_000010.10:g.96748682A>C , CM000672.1:g.96748682A>C | GRCh37 |
NC_000010.9:g.96738672A>C | NCBI36 |
NG_008385.1:g.55268A>C | |
NG_008385.2:g.55768A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.1370A>C MANE Select | ENSP00000260682.6:p.Asn457Thr | |
ENST00000643112.1:c.*379A>C | ENSP00000496202.1:n.*379A>C | |
ENST00000260682.6:c.1370A>C | ENSP00000260682.6:p.Asn457Thr | |
NM_000771.3:c.1370A>C | NP_000762.2:p.Asn457Thr | |
NM_000771.4:c.1370A>C MANE Select | NP_000762.2:p.Asn457Thr |