Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38145292A>G , CM000670.2:g.38145292A>G | GRCh38 |
| NC_000008.10:g.38002810A>G , CM000670.1:g.38002810A>G | GRCh37 |
| NC_000008.9:g.38121967A>G | NCBI36 |
| NG_011827.1:g.10791T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000349.3:c.674T>C MANE Select | NP_000340.2:p.Met225Thr |
| ENST00000276449.9:c.674T>C MANE Select | ENSP00000276449.3:p.Met225Thr |
| NM_000349.2:c.674T>C | NP_000340.2:p.Met225Thr |
| ENST00000276449.8:c.674T>C | ENSP00000276449.3:p.Met225Thr |
| ENST00000520114.1:n.1808T>C | |
| ENST00000522050.1:c.586+671T>C | |
| XM_006716392.1:c.650+671T>C | XP_006716455.1:n.650+671T>C |