Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585473C= , CM000665.2:g.98585473C= | GRCh38 |
| NC_000003.11:g.98304317C= , CM000665.1:g.98304317C= | GRCh37 |
| NC_000003.10:g.99787007C= | NCBI36 |
| NG_015994.1:g.13139G= | |
| NG_015994.2:g.13139G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000512905.6:c.26G= | ||
| ENST00000647941.2:c.1140G= MANE Select | ENSP00000497326.1:p.Gln380= | |
| ENST00000264193.2:c.1140G= | ENSP00000264193.2:p.Gln380= | |
| ENST00000510489.1:n.390G= | ||
| ENST00000512905.5:c.26G= | ||
| NM_000097.5:c.1140G= | NP_000088.3:p.Gln380= | |
| XM_005247125.3:c.1140G= | XP_005247182.1:p.Gln380= | |
| NM_000097.7:c.1140G= MANE Select | NP_000088.3:p.Gln380= | |
| XM_005247125.4:c.1140G= | XP_005247182.1:p.Gln380= | |
| XR_001740025.2:n.1311G= | ||
| XR_001740026.1:n.1875G= | ||
| XR_001740027.1:n.1415G= | ||
| XR_001740028.1:n.1381G= |