Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7533471C>T , CM000681.2:g.7533471C>T | GRCh38 |
| NC_000019.9:g.7598357C>T , CM000681.1:g.7598357C>T | GRCh37 |
| NC_000019.8:g.7504357C>T | NCBI36 |
| NG_013374.1:g.4320C>T | |
| NG_015806.1:g.15862C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264079.11:c.1576-52C>T MANE Select | ENSP00000264079.5:n.1576-52C>T | |
| ENST00000264079.10:c.1576-52C>T | ENSP00000264079.5:n.1576-52C>T | |
| ENST00000394321.9:n.1891-52C>T | ||
| ENST00000599334.1:c.304-52C>T | ||
| ENST00000602227.1:n.78C>T | ||
| NM_020533.2:c.1576-52C>T | NP_065394.1:n.1576-52C>T | |
| NM_020533.3:c.1576-52C>T MANE Select | NP_065394.1:n.1576-52C>T |