HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786173A= , CM000681.2:g.18786173A= | GRCh38 |
NC_000019.9:g.18896983A= , CM000681.1:g.18896983A= | GRCh37 |
NC_000019.8:g.18757983A= | NCBI36 |
NG_007070.1:g.10132T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000222271.7:c.1308-27T= MANE Select | ENSP00000222271.2:n.1308-27T= | |
ENST00000222271.6:c.1308-27T= | ENSP00000222271.2:n.1308-27T= | |
ENST00000425807.1:c.1149-27T= | ENSP00000403792.1:n.1149-27T= | |
ENST00000542601.6:c.1209-27T= | ENSP00000439156.2:n.1209-27T= | |
ENST00000612179.1:n.558-27T= | ||
NM_000095.2:c.1308-27T= | NP_000086.2:n.1308-27T= | |
NM_000095.3:c.1308-27T= MANE Select | NP_000086.2:n.1308-27T= |