HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153690504A>T , CM000685.2:g.153690504A>T | GRCh38 |
NC_000023.10:g.152955959A>T , CM000685.1:g.152955959A>T | GRCh37 |
NC_000023.9:g.152609153A>T | NCBI36 |
NG_012016.1:g.7208A>T | |
NG_012016.2:g.7208A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253122.10:c.392A>T MANE Select | ENSP00000253122.5:p.Lys131Ile | |
ENST00000675713.1:n.146A>T | ||
ENST00000253122.9:c.392A>T | ENSP00000253122.5:p.Lys131Ile | |
ENST00000430077.6:c.47A>T | ENSP00000403041.2:p.Lys16Ile | |
ENST00000476466.1:n.244A>T | ||
NM_001142805.1:c.392A>T | NP_001136277.1:p.Lys131Ile | |
NM_001142806.1:c.47A>T | NP_001136278.1:p.Lys16Ile | |
NM_005629.3:c.392A>T | NP_005620.1:p.Lys131Ile | |
NM_005629.4:c.392A>T MANE Select | NP_005620.1:p.Lys131Ile | |
NM_001142805.2:c.392A>T | NP_001136277.1:p.Lys131Ile |