Linked Data
dbSNP Id:
rs1377479855
gnomAD v2:
17-42085057-C-T
gnomAD v3:
17-44007689-C-T
gnomAD v4:
17-44007689-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44007689C>T , CM000679.2:g.44007689C>T | GRCh38 |
| NC_000017.10:g.42085057C>T , CM000679.1:g.42085057C>T | GRCh37 |
| NC_000017.9:g.39440583C>T | NCBI36 |
| NG_008106.1:g.8026C>T | |
| NG_023338.1:g.1781G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293404.8:c.1367C>T (NAGS) MANE Select | ENSP00000293404.2:p.Ser456Phe | |
| ENST00000293404.7:c.1367C>T (NAGS) | ENSP00000293404.2:p.Ser456Phe | |
| ENST00000589767.1:c.1298C>T (NAGS) | ENSP00000465408.1:p.Ser433Phe | |
| ENST00000592915.1:n.1255C>T (NAGS) | ||
| NM_153006.2:c.1367C>T (NAGS) | NP_694551.1:p.Ser456Phe | |
| XM_011524438.1:c.1268+195C>T (NAGS) | XP_011522740.1:n.1268+195C>T | |
| XM_011524439.1:c.869C>T (NAGS) | XP_011522741.1:p.Ser290Phe | |
| XM_011525035.1:c.-463+15883G>A (PYY) | XP_011523337.1:n.-463+15883G>A | |
| XM_011524439.2:c.869C>T (NAGS) | XP_011522741.1:p.Ser290Phe | |
| NM_153006.3:c.1367C>T (NAGS) MANE Select | NP_694551.1:p.Ser456Phe |