Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4899381G= , CM000679.2:g.4899381G= | GRCh38 |
| NC_000017.10:g.4802676G= , CM000679.1:g.4802676G= | GRCh37 |
| NC_000017.9:g.4743455G= | NCBI36 |
| NG_008029.2:g.8695C= | |
| NG_028005.1:g.71042G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649488.2:c.1036C= MANE Select | ENSP00000497829.1:p.Leu346= | |
| ENST00000649830.1:c.103C= | ENSP00000496907.1:p.Leu35= | |
| ENST00000652550.1:n.766C= | ||
| ENST00000293780.4:c.1036C= | ENSP00000293780.4:p.Leu346= | |
| ENST00000572438.1:n.722C= | ||
| NM_000080.3:c.1036C= | NP_000071.1:p.Leu346= | |
| NM_000080.4:c.1036C= MANE Select | NP_000071.1:p.Leu346= | |
| XM_017024115.1:c.1000C= | XP_016879604.1:p.Leu334= | |
| XR_001752421.1:n.1766C= |