HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877674G= , CM000670.2:g.6877674G= | GRCh38 |
NC_000008.10:g.6735196G= , CM000670.1:g.6735196G= | GRCh37 |
NC_000008.9:g.6722606G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297439.4:c.61+123C= MANE Select | ENSP00000297439.3:n.61+123C= | |
ENST00000297439.3:c.61+123C= | ENSP00000297439.3:n.61+123C= | |
NM_005218.3:c.61+123C= | NP_005209.1:n.61+123C= | |
NM_005218.4:c.61+123C= MANE Select | NP_005209.1:n.61+123C= |