Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837612T>A , CM000685.2:g.154837612T>A | GRCh38 |
| NC_000023.10:g.154065887T>A , CM000685.1:g.154065887T>A | GRCh37 |
| NC_000023.9:g.153719081T>A | NCBI36 |
| NG_011403.1:g.190112A>T | |
| NG_033065.1:g.2051A>T | |
| NG_011403.2:g.190112A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.7041A>T MANE Select | NP_000123.1:p.Ala2347= |
| ENST00000360256.9:c.7041A>T MANE Select | ENSP00000353393.4:p.Ala2347= |
| NM_000132.3:c.7041A>T | NP_000123.1:p.Ala2347= |
| NM_019863.2:c.636A>T | NP_063916.1:p.Ala212= |
| NM_019863.3:c.636A>T | NP_063916.1:p.Ala212= |
| ENST00000330287.10:c.636A>T | ENSP00000327895.6:p.Ala212= |
| ENST00000360256.8:c.7041A>T | ENSP00000353393.4:p.Ala2347= |
| ENST00000644698.1:c.774A>T | ENSP00000495706.1:p.Ala258= |
| XM_011531126.1:c.6936A>T | XP_011529428.1:p.Ala2312= |