HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74754842C>T , CM000677.2:g.74754842C>T | GRCh38 |
NC_000015.9:g.75047183C>T , CM000677.1:g.75047183C>T | GRCh37 |
NC_000015.8:g.72834236C>T | NCBI36 |
NG_008431.1:g.37301C>T | |
NG_008431.2:g.37301C>T | |
NG_061543.1:g.10998C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.1305C>T MANE Select | ENSP00000342007.4:p.Ala435= | |
ENST00000343932.4:c.1305C>T | ENSP00000342007.4:p.Ala435= | |
NM_000761.4:c.1305C>T | NP_000752.2:p.Ala435= | |
NM_000761.5:c.1305C>T MANE Select | NP_000752.2:p.Ala435= |