Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965794G= , CM000670.2:g.37965794G= | GRCh38 |
| NC_000008.10:g.37823312G= , CM000670.1:g.37823312G= | GRCh37 |
| NC_000008.9:g.37942469G= | NCBI36 |
| NG_011936.1:g.5873C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.676C= MANE Select | NP_000016.1:p.Arg226= |
| ENST00000345060.5:c.676C= MANE Select | ENSP00000343782.3:p.Arg226= |
| NM_000025.2:c.676C= | NP_000016.1:p.Arg226= |
| ENST00000345060.4:c.676C= | ENSP00000343782.3:p.Arg226= |
| ENST00000520341.2:n.804C= | |
| ENST00000614635.1:c.676C= | ENSP00000480325.1:p.Arg226= |
| ENST00000647937.1:c.160C= | ENSP00000497740.1:p.Arg54= |