Linked Data
dbSNP Id:
rs776000137
ExAC:
1:207697054 A / T
gnomAD v2:
1-207697054-A-T
gnomAD v3:
1-207523709-A-T
gnomAD v4:
1-207523709-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207523709A>T , CM000663.2:g.207523709A>T | GRCh38 |
| NC_000001.10:g.207697054A>T , CM000663.1:g.207697054A>T | GRCh37 |
| NC_000001.9:g.205763677A>T | NCBI36 |
| NG_007481.1:g.32582A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367049.9:c.586A>T MANE Select | ENSP00000356016.4:p.Asn196Tyr | |
| ENST00000367051.6:c.487+12055A>T | ENSP00000356018.1:n.487+12055A>T | |
| ENST00000367052.6:c.586A>T | ENSP00000356019.1:p.Asn196Tyr | |
| ENST00000367053.6:c.586A>T | ENSP00000356020.1:p.Asn196Tyr | |
| ENST00000400960.7:c.586A>T | ENSP00000383744.2:p.Asn196Tyr | |
| ENST00000367049.8:c.586A>T | ENSP00000356016.4:p.Asn196Tyr | |
| ENST00000367050.8:n.707A>T | ||
| ENST00000367051.5:c.487+12055A>T | ENSP00000356018.1:n.487+12055A>T | |
| ENST00000367052.5:c.586A>T | ENSP00000356019.1:p.Asn196Tyr | |
| ENST00000367053.5:c.586A>T | ENSP00000356020.1:p.Asn196Tyr | |
| ENST00000400960.6:c.586A>T | ENSP00000383744.2:p.Asn196Tyr | |
| ENST00000434033.5:n.513A>T | ||
| ENST00000436595.1:n.414+12055A>T | ||
| ENST00000450439.5:n.513A>T | ||
| ENST00000529814.1:c.513A>T | ||
| ENST00000534202.5:c.586A>T | ENSP00000436139.2:p.Asn196Tyr | |
| NM_000573.3:c.586A>T | NP_000564.2:p.Asn196Tyr | |
| NM_000651.4:c.586A>T | NP_000642.3:p.Asn196Tyr | |
| XM_006711166.2:c.601A>T | XP_006711229.1:p.Asn201Tyr | |
| XM_011509205.1:c.601A>T | XP_011507507.1:p.Asn201Tyr | |
| NM_000651.5:c.586A>T | NP_000642.3:p.Asn196Tyr | |
| XM_024453287.1:c.601A>T | XP_024309055.1:p.Asn201Tyr | |
| NM_000573.4:c.586A>T | NP_000564.2:p.Asn196Tyr | |
| NM_000651.6:c.586A>T MANE Select | NP_000642.3:p.Asn196Tyr |