HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767623C= , CM000676.2:g.28767623C= | GRCh38 |
NC_000014.8:g.29236829C= , CM000676.1:g.29236829C= | GRCh37 |
NC_000014.7:g.28306580C= | NCBI36 |
NG_009367.1:g.5543C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.344C= | ENSP00000516406.1:p.Ala115= | |
ENST00000313071.7:c.344C= MANE Select | ENSP00000339004.3:p.Ala115= | |
ENST00000313071.6:c.344C= | ENSP00000339004.3:p.Ala115= | |
NM_005249.4:c.344C= | NP_005240.3:p.Ala115= | |
NM_005249.5:c.344C= MANE Select | NP_005240.3:p.Ala115= |