Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680288C>T , CM000663.2:g.186680288C>T | GRCh38 |
| NC_000001.10:g.186649420C>T , CM000663.1:g.186649420C>T | GRCh37 |
| NC_000001.9:g.184916043C>T | NCBI36 |
| NG_028206.2:g.5140G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000963.4:c.3G>A MANE Select | NP_000954.1:p.Met1Ile |
| ENST00000367468.10:c.3G>A MANE Select | ENSP00000356438.5:p.Met1Ile |
| NM_000963.3:c.3G>A | NP_000954.1:p.Met1Ile |
| ENST00000367468.9:c.3G>A | ENSP00000356438.5:p.Met1Ile |
| ENST00000490885.6:n.136G>A | |
| ENST00000559627.1:c.3G>A | ENSP00000454130.1:p.Met1Ile |
| ENST00000559800.1:n.136G>A | |
| ENST00000680451.1:c.3G>A | ENSP00000506242.1:p.Met1Ile |
| ENST00000681605.1:c.3G>A | ENSP00000504900.1:p.Met1Ile |