Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.147824702G= , CM000667.2:g.147824702G= | GRCh38 |
| NC_000005.9:g.147204265G= , CM000667.1:g.147204265G= | GRCh37 |
| NC_000005.8:g.147184458G= | NCBI36 |
| NG_008356.2:g.19530C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296695.10:c.199C= MANE Select | ENSP00000296695.5:p.Arg67= | |
| ENST00000296695.9:c.199C= | ENSP00000296695.5:p.Arg67= | |
| ENST00000505722.1:n.114C= | ||
| NM_003122.4:c.199C= | NP_003113.2:p.Arg67= | |
| NM_001354966.1:c.199C= | NP_001341895.1:p.Arg67= | |
| NM_001354966.2:c.199C= | NP_001341895.1:p.Arg67= | |
| NM_001379610.1:c.199C= MANE Select | NP_001366539.1:p.Arg67= | |
| NM_003122.5:c.199C= | NP_003113.2:p.Arg67= |