Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29228996G>C , CM000664.2:g.29228996G>C | GRCh38 |
| NC_000002.11:g.29451862G>C , CM000664.1:g.29451862G>C | GRCh37 |
| NC_000002.10:g.29305366G>C | NCBI36 |
| NG_009445.1:g.697571C>G , LRG_488:g.697571C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.2703C>G MANE Select | NP_004295.2:p.Thr901= |
| ENST00000389048.8:c.2703C>G MANE Select | ENSP00000373700.3:p.Thr901= |
| NM_004304.4:c.2703C>G | NP_004295.2:p.Thr901= |
| ENST00000389048.7:c.2703C>G | ENSP00000373700.3:p.Thr901= |
| ENST00000618119.4:c.1572C>G | ENSP00000482733.1:p.Thr524= |
| XM_024452778.1:c.-71C>G | XP_024308546.1:n.-71C>G |
| XR_001738688.2:n.3633C>G |