Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32589729T>A , CM000668.2:g.32589729T>A | GRCh38 |
| NC_000006.11:g.32557506T>A , CM000668.1:g.32557506T>A | GRCh37 |
| NC_000006.10:g.32665484T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002124.4:c.14A>T MANE Select | NP_002115.2:p.Lys5Met |
| ENST00000360004.6:c.14A>T MANE Select | ENSP00000353099.5:p.Lys5Met |
| NM_002124.3:c.14A>T | NP_002115.2:p.Lys5Met |
| ENST00000360004.5:c.14A>T | ENSP00000353099.5:p.Lys5Met |
| ENST00000611060.4:c.14A>T | ENSP00000480667.1:p.Lys5Met |
| ENST00000696610.1:c.14A>T | ENSP00000512754.1:p.Lys5Met |
| ENST00000696612.1:n.77A>T |