Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713254T>G , CM000681.2:g.6713254T>G | GRCh38 |
| NC_000019.9:g.6713265T>G , CM000681.1:g.6713265T>G | GRCh37 |
| NC_000019.8:g.6664265T>G | NCBI36 |
| NG_009557.1:g.12398A>C , LRG_27:g.12398A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.815A>C | ENSP00000512083.1:p.Asn272Thr | |
| ENST00000695654.1:c.62A>C | ENSP00000512085.1:p.Asn21Thr | |
| ENST00000695692.1:n.262A>C | ||
| ENST00000245907.11:c.938A>C MANE Select | ENSP00000245907.4:p.Asn313Thr | |
| ENST00000245907.10:c.938A>C | ENSP00000245907.4:p.Asn313Thr | |
| ENST00000594270.5:n.62A>C | ||
| ENST00000595577.1:n.442A>C | ||
| ENST00000597442.5:n.188A>C | ||
| NM_000064.3:c.938A>C | NP_000055.2:p.Asn313Thr | |
| NM_000064.4:c.938A>C MANE Select | NP_000055.2:p.Asn313Thr |