Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.53560657A= , CM000667.2:g.53560657A= | GRCh38 |
| NC_000005.9:g.52856487A= , CM000667.1:g.52856487A= | GRCh37 |
| NC_000005.8:g.52892244A= | NCBI36 |
| NG_008200.1:g.5023A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296684.10:c.-6A= MANE Select | ENSP00000296684.5:n.-6A= | |
| ENST00000296684.9:c.-6A= | ENSP00000296684.5:n.-6A= | |
| ENST00000502423.5:c.-6A= | ENSP00000422177.1:n.-6A= | |
| ENST00000506974.5:c.-6A= | ENSP00000425967.1:n.-6A= | |
| ENST00000507026.5:c.-6A= | ENSP00000424993.1:n.-6A= | |
| NM_002495.2:c.-6A= | NP_002486.1:n.-6A= | |
| XM_005248525.3:c.-6A= | XP_005248582.1:n.-6A= | |
| XM_011543414.1:c.-6A= | XP_011541716.1:n.-6A= | |
| NM_001318051.1:c.-6A= | NP_001304980.1:n.-6A= | |
| NM_002495.3:c.-6A= | NP_002486.1:n.-6A= | |
| NR_134473.1:n.25A= | ||
| NR_134474.1:n.25A= | ||
| NR_134475.1:n.25A= | ||
| XM_017009491.1:c.-6A= | XP_016864980.1:n.-6A= | |
| NM_002495.4:c.-6A= MANE Select | NP_002486.1:n.-6A= | |
| NM_001318051.2:c.-6A= | NP_001304980.1:n.-6A= | |
| NR_134473.2:n.19A= | ||
| NR_134474.2:n.19A= | ||
| NR_134475.2:n.19A= |