HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2843337T= , CM000686.2:g.2843337T= | GRCh38 |
NC_000024.9:g.2711378T= , CM000686.1:g.2711378T= | GRCh37 |
NC_000024.8:g.2771378T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679518.1:n.327-740T= | ||
ENST00000681787.1:n.383-740T= | ||
ENST00000681940.1:n.107-2309T= | ||
ENST00000250784.13:c.82-740T= MANE Select | ENSP00000250784.7:n.82-740T= | |
ENST00000250784.12:c.82-740T= | ENSP00000250784.7:n.82-740T= | |
ENST00000430575.1:c.109-740T= | ENSP00000415317.1:n.109-740T= | |
NM_001008.3:c.82-740T= | NP_000999.1:n.82-740T= | |
NM_001008.4:c.82-740T= MANE Select | NP_000999.1:n.82-740T= |