HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19958048C= , CM000670.2:g.19958048C= | GRCh38 |
NC_000008.10:g.19815559C= , CM000670.1:g.19815559C= | GRCh37 |
NC_000008.9:g.19859839C= | NCBI36 |
NG_008855.1:g.23978C= | |
NG_008855.2:g.61332C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1019-1212C= MANE Select | ENSP00000497642.1:n.1019-1212C= | |
ENST00000650478.1:c.79+1965C= | ENSP00000497560.1:n.79+1965C= | |
ENST00000311322.8:c.1019-1212C= | ENSP00000309757.6:n.1019-1212C= | |
NM_000237.2:c.1019-1212C= | NP_000228.1:n.1019-1212C= | |
NM_000237.3:c.1019-1212C= MANE Select | NP_000228.1:n.1019-1212C= |