Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42698381A>G , CM000668.2:g.42698381A>G | GRCh38 |
| NC_000006.11:g.42666119A>G , CM000668.1:g.42666119A>G | GRCh37 |
| NC_000006.10:g.42774097A>G | NCBI36 |
| NG_009176.1:g.29240T>C | |
| NG_009176.2:g.29240T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000322.5:c.955T>C MANE Select | NP_000313.2:p.Phe319Leu |
| ENST00000230381.7:c.955T>C MANE Select | ENSP00000230381.5:p.Phe319Leu |
| NM_000322.4:c.955T>C | NP_000313.2:p.Phe319Leu |
| ENST00000230381.6:c.955T>C | ENSP00000230381.5:p.Phe319Leu |
| XR_926295.3:n.1842T>C |