HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786193T= , CM000681.2:g.18786193T= | GRCh38 |
NC_000019.9:g.18897003T= , CM000681.1:g.18897003T= | GRCh37 |
NC_000019.8:g.18758003T= | NCBI36 |
NG_007070.1:g.10112A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1308-47A= MANE Select | ENSP00000222271.2:n.1308-47A= | |
ENST00000222271.6:c.1308-47A= | ENSP00000222271.2:n.1308-47A= | |
ENST00000425807.1:c.1149-47A= | ENSP00000403792.1:n.1149-47A= | |
ENST00000542601.6:c.1209-47A= | ENSP00000439156.2:n.1209-47A= | |
ENST00000612179.1:n.558-47A= | ||
NM_000095.2:c.1308-47A= | NP_000086.2:n.1308-47A= | |
NM_000095.3:c.1308-47A= MANE Select | NP_000086.2:n.1308-47A= |