Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54456233C= , CM000685.2:g.54456233C= | GRCh38 |
| NC_000023.10:g.54482666C= , CM000685.1:g.54482666C= | GRCh37 |
| NC_000023.9:g.54499391C= | NCBI36 |
| NG_008054.1:g.44934G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004463.3:c.1829G= MANE Select | NP_004454.2:p.Arg610= |
| ENST00000375135.4:c.1829G= MANE Select | ENSP00000364277.3:p.Arg610= |
| NM_004463.2:c.1829G= | NP_004454.2:p.Arg610= |
| ENST00000375135.3:c.1829G= | ENSP00000364277.3:p.Arg610= |