Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219055843C>T , CM000664.2:g.219055843C>T | GRCh38 |
| NC_000002.11:g.219920565C>T , CM000664.1:g.219920565C>T | GRCh37 |
| NC_000002.10:g.219628809C>T | NCBI36 |
| NG_016741.1:g.9674G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002181.4:c.600G>A MANE Select | NP_002172.2:p.Thr200= |
| ENST00000295731.7:c.600G>A MANE Select | ENSP00000295731.5:p.Thr200= |
| NM_002181.3:c.600G>A | NP_002172.2:p.Thr200= |
| ENST00000295731.6:c.600G>A | ENSP00000295731.5:p.Thr200= |