Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2274981T= , CM000681.2:g.2274981T= | GRCh38 |
| NC_000019.9:g.2274980T= , CM000681.1:g.2274980T= | GRCh37 |
| NC_000019.8:g.2225980T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342063.5:c.*699A= MANE Select | ENSP00000345102.3:n.*699A= | |
| ENST00000342063.4:c.*699A= | ENSP00000345102.3:n.*699A= | |
| ENST00000621615.1:c.146+5237T= | ENSP00000481965.1:n.146+5237T= | |
| NM_198532.2:c.*699A= | NP_940934.1:n.*699A= | |
| NM_198532.3:c.*699A= MANE Select | NP_940934.1:n.*699A= |