HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94949051T>C , CM000672.2:g.94949051T>C | GRCh38 |
NC_000010.10:g.96708808T>C , CM000672.1:g.96708808T>C | GRCh37 |
NC_000010.9:g.96698798T>C | NCBI36 |
NG_008385.1:g.15394T>C | |
NG_008385.2:g.15894T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.643-57T>C MANE Select | ENSP00000260682.6:n.643-57T>C | |
ENST00000643112.1:c.643-57T>C | ENSP00000496202.1:n.643-57T>C | |
ENST00000260682.6:c.643-57T>C | ENSP00000260682.6:n.643-57T>C | |
ENST00000473496.1:n.414-57T>C | ||
NM_000771.3:c.643-57T>C | NP_000762.2:n.643-57T>C | |
NM_000771.4:c.643-57T>C MANE Select | NP_000762.2:n.643-57T>C |