Linked Data
dbSNP Id:
rs753464942
ExAC:
17:39742613 C / T
gnomAD v2:
17-39742613-C-T
gnomAD v4:
17-41586361-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41586361C>T , CM000679.2:g.41586361C>T | GRCh38 |
| NC_000017.10:g.39742613C>T , CM000679.1:g.39742613C>T | GRCh37 |
| NC_000017.9:g.36996139C>T | NCBI36 |
| NG_008624.1:g.5535G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.474G>A MANE Select | ENSP00000167586.6:p.Glu158= | |
| ENST00000167586.6:c.474G>A | ENSP00000167586.6:p.Glu158= | |
| NM_000526.4:c.474G>A | NP_000517.2:p.Glu158= | |
| NM_000526.5:c.474G>A MANE Select | NP_000517.3:p.Glu158= |