Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219060086G= , CM000664.2:g.219060086G= | GRCh38 |
| NC_000002.11:g.219924808G= , CM000664.1:g.219924808G= | GRCh37 |
| NC_000002.10:g.219633052G= | NCBI36 |
| NG_016741.1:g.5431C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295731.7:c.315+67C= MANE Select | ENSP00000295731.5:n.315+67C= | |
| ENST00000295731.6:c.315+67C= | ENSP00000295731.5:n.315+67C= | |
| NM_002181.3:c.315+67C= | NP_002172.2:n.315+67C= | |
| NM_002181.4:c.315+67C= MANE Select | NP_002172.2:n.315+67C= |