HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322493T= , CM000677.2:g.73322493T= | GRCh38 |
NC_000015.9:g.73614834T= , CM000677.1:g.73614834T= | GRCh37 |
NC_000015.8:g.71401887T= | NCBI36 |
NG_009063.1:g.51772A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3600A= MANE Select | ENSP00000261917.3:p.Pro1200= | |
ENST00000261917.3:c.3600A= | ENSP00000261917.3:p.Pro1200= | |
NM_005477.2:c.3600A= | NP_005468.1:p.Pro1200= | |
XM_011521148.1:c.2382A= | XP_011519450.1:p.Pro794= | |
XM_011521148.2:c.2382A= | XP_011519450.1:p.Pro794= | |
NM_005477.3:c.3600A= MANE Select | NP_005468.1:p.Pro1200= |