HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7528239C>T , CM000681.2:g.7528239C>T | GRCh38 |
NC_000019.9:g.7593125C>T , CM000681.1:g.7593125C>T | GRCh37 |
NC_000019.8:g.7499125C>T | NCBI36 |
NG_015806.1:g.10630C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.859C>T MANE Select | ENSP00000264079.5:p.Pro287Ser | |
ENST00000264079.10:c.859C>T | ENSP00000264079.5:p.Pro287Ser | |
ENST00000394321.9:n.1174C>T | ||
NM_020533.2:c.859C>T | NP_065394.1:p.Pro287Ser | |
NM_020533.3:c.859C>T MANE Select | NP_065394.1:p.Pro287Ser |