Linked Data
dbSNP Id:
rs1570822471
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119421917A>C , CM000663.2:g.119421917A>C | GRCh38 |
| NC_000001.10:g.119964540A>C , CM000663.1:g.119964540A>C | GRCh37 |
| NC_000001.9:g.119766063A>C | NCBI36 |
| NG_013349.1:g.11987A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.416A>C MANE Select | ENSP00000358424.3:p.Asn139Thr | |
| ENST00000369416.3:c.416A>C | ENSP00000358424.3:p.Asn139Thr | |
| ENST00000433745.5:c.416A>C | ENSP00000388292.1:p.Asn139Thr | |
| ENST00000448448.2:n.360A>C | ||
| ENST00000543831.5:c.416A>C | ENSP00000445122.1:p.Asn139Thr | |
| NM_000198.3:c.416A>C | NP_000189.1:p.Asn139Thr | |
| NM_001166120.1:c.416A>C | NP_001159592.1:p.Asn139Thr | |
| NM_000198.4:c.416A>C MANE Select | NP_000189.1:p.Asn139Thr | |
| NM_001166120.2:c.416A>C | NP_001159592.1:p.Asn139Thr |