dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71979082A>C , CM000674.2:g.71979082A>C | GRCh38 |
| NC_000012.11:g.72372862A>C , CM000674.1:g.72372862A>C | GRCh37 |
| NC_000012.10:g.70659129A>C | NCBI36 |
| NG_008279.1:g.45237A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333850.4:c.936A>C MANE Select | ENSP00000329093.3:p.Pro312= | |
| ENST00000333850.3:c.936A>C | ENSP00000329093.3:p.Pro312= | |
| NM_173353.3:c.936A>C | NP_775489.2:p.Pro312= | |
| XM_011537899.1:c.342A>C | XP_011536201.1:p.Pro114= | |
| NM_173353.4:c.936A>C MANE Select | NP_775489.2:p.Pro312= |