HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954308A>C , CM000670.2:g.19954308A>C | GRCh38 |
NC_000008.10:g.19811819A>C , CM000670.1:g.19811819A>C | GRCh37 |
NC_000008.9:g.19856099A>C | NCBI36 |
NG_008855.1:g.20238A>C | |
NG_008855.2:g.57592A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.730A>C MANE Select | ENSP00000497642.1:p.Asn244His | |
ENST00000311322.8:c.730A>C | ENSP00000309757.6:p.Asn244His | |
NM_000237.2:c.730A>C | NP_000228.1:p.Asn244His | |
NM_000237.3:c.730A>C MANE Select | NP_000228.1:p.Asn244His |