Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541286A>C , CM000680.2:g.31541286A>C | GRCh38 |
| NC_000018.9:g.29121249A>C , CM000680.1:g.29121249A>C | GRCh37 |
| NC_000018.8:g.27375247A>C | NCBI36 |
| NG_007072.3:g.48045A>C , LRG_397:g.48045A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.1973A>C MANE Select | ENSP00000261590.8:p.Asn658Thr | |
| ENST00000261590.12:c.1973A>C | ENSP00000261590.8:p.Asn658Thr | |
| NM_001943.3:c.1973A>C , LRG_397t1:c.1973A>C | NP_001934.2:p.Asn658Thr | |
| NM_001943.4:c.1973A>C | NP_001934.2:p.Asn658Thr | |
| XM_024451095.1:c.1439A>C | XP_024306863.1:p.Asn480Thr | |
| NM_001943.5:c.1973A>C MANE Select | NP_001934.2:p.Asn658Thr |