HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538805C= , CM000672.2:g.133538805C= | GRCh38 |
NC_000010.10:g.135352309C= , CM000672.1:g.135352309C= | GRCh37 |
NC_000010.9:g.135202299C= | NCBI36 |
NG_008383.1:g.16443C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1323C= MANE Select | ENSP00000252945.3:p.Gly441= | |
ENST00000252945.7:c.1323C= | ENSP00000252945.3:p.Gly441= | |
ENST00000368520.1:n.1358+913C= | ||
ENST00000418356.1:c.912C= | ENSP00000397299.1:p.Gly304= | |
ENST00000421586.5:c.1062C= | ENSP00000412754.1:p.Gly354= | |
ENST00000463117.6:c.1323C= | ENSP00000440689.1:p.Gly441= | |
ENST00000469258.1:n.419C= | ||
ENST00000541080.5:c.739C= | ||
NM_000773.3:c.1323C= | NP_000764.1:p.Gly441= | |
NM_000773.4:c.1323C= MANE Select | NP_000764.1:p.Gly441= |