HGVS | Genome Assembly |
---|---|
NC_000002.12:g.5692904G>T , CM000664.2:g.5692904G>T | GRCh38 |
NC_000002.11:g.5833036G>T , CM000664.1:g.5833036G>T | GRCh37 |
NC_000002.10:g.5750487G>T | NCBI36 |
NG_050751.1:g.5238G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000322002.5:c.183G>T MANE Select | ENSP00000322568.3:p.Lys61Asn | |
ENST00000322002.4:c.183G>T | ENSP00000322568.3:p.Lys61Asn | |
NM_003108.3:c.183G>T | NP_003099.1:p.Lys61Asn | |
NM_003108.4:c.183G>T MANE Select | NP_003099.1:p.Lys61Asn |