Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.113074787C>T , CM000664.2:g.113074787C>T | GRCh38 |
| NC_000002.11:g.113832364C>T , CM000664.1:g.113832364C>T | GRCh37 |
| NC_000002.10:g.113548835C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393197.3:c.183C>T | ENSP00000376893.2:p.Ile61= | |
| ENST00000341010.6:c.183C>T MANE Select | ENSP00000341794.2:p.Ile61= | |
| ENST00000393197.2:c.183C>T | ENSP00000376893.2:p.Ile61= | |
| ENST00000496265.1:n.249C>T | ||
| NM_032556.5:c.183C>T | NP_115945.4:p.Ile61= | |
| NM_173161.2:c.183C>T | NP_775184.1:p.Ile61= | |
| NM_032556.6:c.183C>T | NP_115945.4:p.Ile61= | |
| NM_173161.3:c.183C>T MANE Select | NP_775184.1:p.Ile61= |