HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5225603G>T , CM000673.2:g.5225603G>T | GRCh38 |
NC_000011.9:g.5246833G>T , CM000673.1:g.5246833G>T | GRCh37 |
NC_000011.8:g.5203409G>T | NCBI36 |
NG_000007.3:g.72013C>A | |
NG_059281.1:g.6469C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.439C>A | ENSP00000494175.1:p.His147Asn | |
ENST00000335295.4:c.439C>A MANE Select | ENSP00000333994.3:p.His147Asn | |
ENST00000633227.1:c.*255C>A | ENSP00000488004.1:n.*255C>A | |
NM_000518.4:c.439C>A | NP_000509.1:p.His147Asn | |
NM_000518.5:c.439C>A MANE Select | NP_000509.1:p.His147Asn |