HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436619G>C , CM000678.2:g.67436619G>C | GRCh38 |
NC_000016.9:g.67470522G>C , CM000678.1:g.67470522G>C | GRCh37 |
NC_000016.8:g.66028023G>C | NCBI36 |
NG_011482.1:g.49568C>G | |
NG_016549.1:g.10487G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.834G>C MANE Select | ENSP00000316786.5:p.Lys278Asn | |
ENST00000326152.5:c.834G>C | ENSP00000316786.5:p.Lys278Asn | |
NM_000196.3:c.834G>C | NP_000187.3:p.Lys278Asn | |
NM_000196.4:c.834G>C MANE Select | NP_000187.3:p.Lys278Asn |