HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25012754G= , CM000685.2:g.25012754G= | GRCh38 |
NC_000023.10:g.25030871G= , CM000685.1:g.25030871G= | GRCh37 |
NC_000023.9:g.24940792G= | NCBI36 |
NG_008281.1:g.8195C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.1073+168C= MANE Select | ENSP00000368332.4:n.1073+168C= | |
ENST00000379044.4:c.1073+168C= | ENSP00000368332.4:n.1073+168C= | |
NM_139058.2:c.1073+168C= | NP_620689.1:n.1073+168C= | |
NM_139058.3:c.1073+168C= MANE Select | NP_620689.1:n.1073+168C= |