Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17018938A>G , CM000663.2:g.17018938A>G | GRCh38 |
| NC_000001.10:g.17345433A>G , CM000663.1:g.17345433A>G | GRCh37 |
| NC_000001.9:g.17218020A>G | NCBI36 |
| NG_012340.1:g.40233T>C , LRG_316:g.40233T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.615T>C | ENSP00000481376.2:p.Ala205= | |
| ENST00000491274.6:c.744T>C | ENSP00000480482.2:p.Ala248= | |
| ENST00000375499.8:c.786T>C MANE Select | ENSP00000364649.3:p.Ala262= | |
| ENST00000375499.7:c.786T>C | ENSP00000364649.3:p.Ala262= | |
| ENST00000475049.5:n.211T>C | ||
| ENST00000485092.5:n.450T>C | ||
| NM_003000.2:c.786T>C , LRG_316t1:c.786T>C | NP_002991.2:p.Ala262= | |
| NM_003000.3:c.786T>C MANE Select | NP_002991.2:p.Ala262= |