Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162272377C= , CM000664.2:g.162272377C= | GRCh38 |
| NC_000002.11:g.163128887C= , CM000664.1:g.163128887C= | GRCh37 |
| NC_000002.10:g.162837133C= | NCBI36 |
| NG_011495.1:g.51153G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022168.4:c.2465G= MANE Select | NP_071451.2:p.Arg822= |
| ENST00000649979.2:c.2465G= MANE Select | ENSP00000497271.1:p.Arg822= |
| NM_022168.3:c.2465G= | NP_071451.2:p.Arg822= |
| ENST00000263642.2:c.2465G= | ENSP00000263642.2:p.Arg822= |
| ENST00000648433.1:c.2348G= | ENSP00000496816.1:p.Arg783= |
| ENST00000649554.1:n.2075G= | |
| ENST00000679938.1:c.2153G= | ENSP00000505518.1:p.Arg718= |
| ENST00000697291.1:c.*2062G= | ENSP00000513228.1:n.*2062G= |
| XM_011511628.1:c.1748G= | XP_011509930.1:p.Arg583= |