Linked Data
dbSNP Id:
rs370167671
ExAC:
2:233398980 T / C
gnomAD v2:
2-233398980-T-C
gnomAD v3:
2-232534270-T-C
gnomAD v4:
2-232534270-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232534270T>C , CM000664.2:g.232534270T>C | GRCh38 |
| NC_000002.11:g.233398980T>C , CM000664.1:g.233398980T>C | GRCh37 |
| NC_000002.10:g.233107224T>C | NCBI36 |
| NG_008028.1:g.13059T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258385.8:c.1299T>C MANE Select | ENSP00000258385.3:p.Asn433= | |
| ENST00000258385.7:c.1299T>C | ENSP00000258385.3:p.Asn433= | |
| ENST00000441621.6:c.*481T>C | ENSP00000408819.2:n.*481T>C | |
| ENST00000446616.1:c.*940T>C | ENSP00000410801.1:n.*940T>C | |
| ENST00000543200.5:c.1254T>C | ENSP00000438380.1:p.Asn418= | |
| NM_000751.2:c.1299T>C | NP_000742.1:p.Asn433= | |
| NM_001256657.1:c.1254T>C | NP_001243586.1:p.Asn418= | |
| NM_001311195.1:c.717T>C | NP_001298124.1:p.Asn239= | |
| NM_001311196.1:c.996T>C | NP_001298125.1:p.Asn332= | |
| NR_046333.1:c.-4294966252T>C | ||
| NR_046334.1:c.-4294965973T>C | ||
| XM_011510524.1:c.918T>C | XP_011508826.1:p.Asn306= | |
| XM_011510524.2:c.918T>C | XP_011508826.1:p.Asn306= | |
| NM_000751.3:c.1299T>C MANE Select | NP_000742.1:p.Asn433= | |
| NM_001311195.2:c.717T>C | NP_001298124.1:p.Asn239= | |
| NM_001311196.2:c.996T>C | NP_001298125.1:p.Asn332= | |
| NM_001256657.2:c.1254T>C | NP_001243586.1:p.Asn418= |