HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767643G>A , CM000676.2:g.28767643G>A | GRCh38 |
NC_000014.8:g.29236849G>A , CM000676.1:g.29236849G>A | GRCh37 |
NC_000014.7:g.28306600G>A | NCBI36 |
NG_009367.1:g.5563G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.364G>A | ENSP00000516406.1:p.Asp122Asn | |
ENST00000313071.7:c.364G>A MANE Select | ENSP00000339004.3:p.Asp122Asn | |
ENST00000313071.6:c.364G>A | ENSP00000339004.3:p.Asp122Asn | |
NM_005249.4:c.364G>A | NP_005240.3:p.Asp122Asn | |
NM_005249.5:c.364G>A MANE Select | NP_005240.3:p.Asp122Asn |