Linked Data
dbSNP Id:
rs777163714
ExAC:
15:89424591 G / A
gnomAD v2:
15-89424591-G-A
gnomAD v4:
15-88881360-G-A
MyVariant Identifiers:
chr15:g.89424591G>A (hg19)
chr15:g.89424591_89424597delinsACAGCTC (hg19)
chr15:g.88881360G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.88881360G>A , CM000677.2:g.88881360G>A | GRCh38 |
| NC_000015.9:g.89424591G>A , CM000677.1:g.89424591G>A | GRCh37 |
| NC_000015.8:g.87225595G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359595.8:c.490C>T MANE Select | ENSP00000352606.4:p.Arg164Trp | |
| ENST00000359595.7:c.490C>T | ENSP00000352606.3:p.Arg164Trp | |
| ENST00000558770.5:c.490C>T | ENSP00000456458.1:p.Arg164Trp | |
| ENST00000562281.1:c.490C>T | ENSP00000456985.1:p.Arg164Trp | |
| ENST00000562889.5:c.676C>T | ENSP00000457180.1:p.Arg226Trp | |
| ENST00000563808.1:n.592C>T | ||
| NM_001307952.1:c.676C>T | NP_001294881.1:p.Arg226Trp | |
| NM_178232.2:c.490C>T | NP_839946.1:p.Arg164Trp | |
| NM_178232.3:c.490C>T | NP_839946.1:p.Arg164Trp | |
| XM_011521261.1:c.622C>T | XP_011519563.1:p.Arg208Trp | |
| XR_243204.1:n.705C>T | ||
| XR_931756.1:n.811C>T | ||
| XM_017021934.2:c.676C>T | XP_016877423.1:p.Arg226Trp | |
| XM_017021935.2:c.111C>T | XP_016877424.1:p.Cys37= | |
| XM_017021936.2:c.111C>T | XP_016877425.1:p.Cys37= | |
| XR_001751098.2:n.823C>T | ||
| XR_931756.3:n.824C>T | ||
| NM_001307952.2:c.676C>T | NP_001294881.1:p.Arg226Trp | |
| NM_178232.4:c.490C>T MANE Select | NP_839946.1:p.Arg164Trp |