Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.74696784G>A , CM000667.2:g.74696784G>A | GRCh38 |
| NC_000005.9:g.73992609G>A , CM000667.1:g.73992609G>A | GRCh37 |
| NC_000005.8:g.74028365G>A | NCBI36 |
| NG_009770.1:g.16641G>A | |
| NG_009770.2:g.61762G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261416.12:c.558+45G>A MANE Select | ENSP00000261416.7:n.558+45G>A | |
| ENST00000261416.11:c.558+45G>A | ENSP00000261416.7:n.558+45G>A | |
| ENST00000510820.1:n.277+45G>A | ||
| ENST00000511181.5:c.-118+45G>A | ENSP00000426285.1:n.-118+45G>A | |
| ENST00000513079.5:n.623+45G>A | ||
| NM_000521.3:c.558+45G>A | NP_000512.1:n.558+45G>A | |
| NM_001292004.1:c.-118+45G>A | NP_001278933.1:n.-118+45G>A | |
| NM_000521.4:c.558+45G>A MANE Select | NP_000512.2:n.558+45G>A | |
| NM_001292004.2:c.-118+45G>A | NP_001278933.1:n.-118+45G>A |