Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47834480G>C , CM000681.2:g.47834480G>C | GRCh38 |
| NC_000019.9:g.48337737G>C , CM000681.1:g.48337737G>C | GRCh37 |
| NC_000019.8:g.53029549G>C | NCBI36 |
| NG_008605.1:g.17639G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000554.6:c.37G>C MANE Select | NP_000545.1:p.Val13Leu |
| ENST00000221996.12:c.37G>C MANE Select | ENSP00000221996.5:p.Val13Leu |
| NM_000554.4:c.37G>C | NP_000545.1:p.Val13Leu |
| NM_000554.5:c.37G>C | NP_000545.1:p.Val13Leu |
| ENST00000221996.11:c.37G>C | ENSP00000221996.5:p.Val13Leu |
| ENST00000539067.5:c.37G>C | ENSP00000445565.1:p.Val13Leu |
| ENST00000556527.1:n.78-1763G>C | |
| ENST00000566686.5:c.37G>C | ENSP00000457808.2:p.Val13Leu |
| ENST00000613299.1:c.37G>C | ENSP00000478106.1:p.Val13Leu |