Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55007141G>A , CM000663.2:g.55007141G>A | GRCh38 |
| NC_000001.10:g.55472814G>A , CM000663.1:g.55472814G>A | GRCh37 |
| NC_000001.9:g.55245402G>A | NCBI36 |
| NG_008965.1:g.13198G>A | |
| NG_008965.2:g.13209G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_057176.3:c.417G>A MANE Select | NP_476517.1:p.Pro139= |
| ENST00000651561.1:c.417G>A MANE Select | ENSP00000498282.1:p.Pro139= |
| NM_057176.2:c.417G>A | NP_476517.1:p.Pro139= |
| ENST00000371265.4:c.417G>A | ENSP00000360312.4:p.Pro139= |
| XM_006710883.2:c.186G>A | XP_006710946.1:p.Pro62= |