Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94425654C>T , CM000669.2:g.94425654C>T | GRCh38 |
| NC_000007.13:g.94054966C>T , CM000669.1:g.94054966C>T | GRCh37 |
| NC_000007.12:g.93892902C>T | NCBI36 |
| NG_007405.1:g.36094C>T , LRG_2:g.36094C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2826C>T MANE Select | NP_000080.2:p.Pro942= |
| ENST00000297268.11:c.2826C>T MANE Select | ENSP00000297268.6:p.Pro942= |
| NM_000089.3:c.2826C>T , LRG_2t1:c.2826C>T | NP_000080.2:p.Pro942= |
| ENST00000297268.10:c.2826C>T | ENSP00000297268.6:p.Pro942= |
| ENST00000469732.1:n.609C>T | |
| ENST00000478215.1:n.385C>T | |
| ENST00000481570.5:n.2799C>T | |
| ENST00000620463.1:c.2820C>T | ENSP00000477719.1:p.Pro940= |