Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152676078A>G , CM000669.2:g.152676078A>G | GRCh38 |
| NC_000007.13:g.152373163A>G , CM000669.1:g.152373163A>G | GRCh37 |
| NC_000007.12:g.152004096A>G | NCBI36 |
| NG_027988.1:g.5088T>C | |
| NG_027988.2:g.5088T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.-85T>C | ENSP00000513758.1:n.-85T>C | |
| ENST00000698507.1:n.70T>C | ||
| ENST00000359321.2:c.2T>C MANE Select | ENSP00000352271.1:p.Met1Thr | |
| ENST00000359321.1:c.2T>C | ENSP00000352271.1:p.Met1Thr | |
| NM_005431.1:c.2T>C | NP_005422.1:p.Met1Thr | |
| NM_005431.2:c.2T>C MANE Select | NP_005422.1:p.Met1Thr |