Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44374717T>G , CM000679.2:g.44374717T>G | GRCh38 |
| NC_000017.10:g.42452085T>G , CM000679.1:g.42452085T>G | GRCh37 |
| NC_000017.9:g.39807611T>G | NCBI36 |
| NG_008331.1:g.19789A>C , LRG_479:g.19789A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.2885A>C MANE Select | ENSP00000262407.5:p.Asn962Thr | |
| ENST00000648408.1:c.2316A>C | ||
| ENST00000262407.5:c.2885A>C | ENSP00000262407.5:p.Asn962Thr | |
| ENST00000587295.5:c.253+1116A>C | ||
| ENST00000592462.5:n.2396A>C | ||
| NM_000419.3:c.2885A>C , LRG_479t1:c.2885A>C | NP_000410.2:p.Asn962Thr | |
| XM_011524749.1:c.2842-247A>C | XP_011523051.1:n.2842-247A>C | |
| XM_011524750.1:c.2885A>C | XP_011523052.1:p.Asn962Thr | |
| NM_000419.4:c.2885A>C | NP_000410.2:p.Asn962Thr | |
| NM_000419.5:c.2885A>C MANE Select | NP_000410.2:p.Asn962Thr |