Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124327A>G , CM000664.2:g.71124327A>G | GRCh38 |
| NC_000002.11:g.71351457A>G , CM000664.1:g.71351457A>G | GRCh37 |
| NC_000002.10:g.71204965A>G | NCBI36 |
| NG_008977.1:g.10938T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.257T>C MANE Select | ENSP00000244217.5:p.Val86Ala | |
| ENST00000244217.5:c.257T>C | ENSP00000244217.5:p.Val86Ala | |
| ENST00000413592.5:c.84+41T>C | ENSP00000391140.1:n.84+41T>C | |
| ENST00000486135.1:c.-29T>C | ENSP00000441569.1:n.-29T>C | |
| ENST00000494660.6:c.-29T>C | ENSP00000437361.1:n.-29T>C | |
| NM_032601.3:c.257T>C | NP_115990.3:p.Val86Ala | |
| XM_005264613.2:c.216+41T>C | XP_005264670.1:n.216+41T>C | |
| XR_939729.1:n.326T>C | ||
| XR_939729.2:n.326T>C | ||
| NM_032601.4:c.257T>C MANE Select | NP_115990.3:p.Val86Ala |