Linked Data
ClinVar Variation Id:
227537
dbSNP Id:
rs876657503
gnomAD v2:
15-66679724-G-A
gnomAD v4:
15-66387386-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66387386G>A , CM000677.2:g.66387386G>A | GRCh38 |
| NC_000015.9:g.66679724G>A , CM000677.1:g.66679724G>A | GRCh37 |
| NC_000015.8:g.64466778G>A | NCBI36 |
| NG_008305.1:g.5514G>A , LRG_725:g.5514G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685172.1:c.39G>A | ENSP00000509604.1:p.Pro13= | |
| ENST00000685763.1:c.39G>A | ENSP00000509016.1:p.Pro13= | |
| ENST00000686347.1:c.39G>A | ENSP00000509027.1:p.Pro13= | |
| ENST00000687191.1:n.475G>A | ||
| ENST00000689951.1:c.39G>A | ENSP00000509308.1:p.Pro13= | |
| ENST00000691077.1:c.39G>A | ENSP00000509843.1:p.Pro13= | |
| ENST00000691576.1:c.39G>A | ENSP00000510066.1:p.Pro13= | |
| ENST00000691937.1:c.39G>A | ENSP00000508768.1:p.Pro13= | |
| ENST00000692487.1:c.39G>A | ENSP00000509534.1:p.Pro13= | |
| ENST00000307102.10:c.39G>A MANE Select | ENSP00000302486.5:p.Pro13= | |
| ENST00000307102.9:c.39G>A | ENSP00000302486.4:p.Pro13= | |
| ENST00000425818.2:n.550G>A | ||
| NM_002755.3:c.39G>A , LRG_725t1:c.39G>A | NP_002746.1:p.Pro13= | |
| XM_017022411.2:c.39G>A | XP_016877900.1:p.Pro13= | |
| NM_002755.4:c.39G>A MANE Select | NP_002746.1:p.Pro13= |