Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659099A>C , CM000685.2:g.136659099A>C | GRCh38 |
| NC_000023.10:g.135741258A>C , CM000685.1:g.135741258A>C | GRCh37 |
| NC_000023.9:g.135568924A>C | NCBI36 |
| NG_007280.1:g.15923A>C , LRG_141:g.15923A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695724.1:c.*88A>C | ENSP00000512122.1:n.*88A>C | |
| ENST00000695725.1:c.*25A>C | ENSP00000512123.1:n.*25A>C | |
| ENST00000695726.1:n.2438A>C | ||
| ENST00000695729.1:n.3273A>C | ||
| ENST00000370629.7:c.470A>C MANE Select | ENSP00000359663.2:p.Asn157Thr | |
| ENST00000370628.2:c.407A>C | ENSP00000359662.2:p.Asn136Thr | |
| ENST00000370629.6:c.470A>C | ENSP00000359663.2:p.Asn157Thr | |
| NM_000074.2:c.470A>C , LRG_141t1:c.470A>C | NP_000065.1:p.Asn157Thr | |
| NM_000074.3:c.470A>C MANE Select | NP_000065.1:p.Asn157Thr |