HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153690474T>C , CM000685.2:g.153690474T>C | GRCh38 |
NC_000023.10:g.152955929T>C , CM000685.1:g.152955929T>C | GRCh37 |
NC_000023.9:g.152609123T>C | NCBI36 |
NG_012016.1:g.7178T>C | |
NG_012016.2:g.7178T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253122.10:c.362T>C MANE Select | ENSP00000253122.5:p.Ile121Thr | |
ENST00000675713.1:n.116T>C | ||
ENST00000253122.9:c.362T>C | ENSP00000253122.5:p.Ile121Thr | |
ENST00000430077.6:c.17T>C | ENSP00000403041.2:p.Ile6Thr | |
ENST00000476466.1:n.214T>C | ||
NM_001142805.1:c.362T>C | NP_001136277.1:p.Ile121Thr | |
NM_001142806.1:c.17T>C | NP_001136278.1:p.Ile6Thr | |
NM_005629.3:c.362T>C | NP_005620.1:p.Ile121Thr | |
NM_005629.4:c.362T>C MANE Select | NP_005620.1:p.Ile121Thr | |
NM_001142805.2:c.362T>C | NP_001136277.1:p.Ile121Thr |