HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75009086A= , CM000676.2:g.75009086A= | GRCh38 |
NC_000014.8:g.75475789A= , CM000676.1:g.75475789A= | GRCh37 |
NC_000014.7:g.74545542A= | NCBI36 |
NG_013333.1:g.11178A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266126.10:c.954A= MANE Select | ENSP00000266126.5:p.Pro318= | |
ENST00000266126.9:c.954A= | ENSP00000266126.5:p.Pro318= | |
ENST00000556668.1:n.534A= | ||
NM_014239.3:c.954A= | NP_055054.1:p.Pro318= | |
NM_014239.4:c.954A= MANE Select | NP_055054.1:p.Pro318= |