HGVS | Genome Assembly |
---|---|
NC_000023.11:g.48528185G= , CM000685.2:g.48528185G= | GRCh38 |
NC_000023.10:g.48386573G= , CM000685.1:g.48386573G= | GRCh37 |
NC_000023.9:g.48271517G= | NCBI36 |
NG_007452.1:g.11410G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000495186.6:c.470-49G= MANE Select | ENSP00000417052.1:n.470-49G= | |
ENST00000651615.1:c.469+900G= | ENSP00000498524.1:n.469+900G= | |
ENST00000276096.10:n.428-49G= | ||
ENST00000446158.5:c.470-49G= | ENSP00000390031.1:n.470-49G= | |
ENST00000495186.5:c.470-49G= | ENSP00000417052.1:n.470-49G= | |
ENST00000498425.1:n.591-49G= | ||
NM_006579.2:c.470-49G= | NP_006570.1:n.470-49G= | |
NM_006579.3:c.470-49G= MANE Select | NP_006570.1:n.470-49G= |