Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.219060565G= , CM000664.2:g.219060565G= | GRCh38 |
| NC_000002.11:g.219925287G= , CM000664.1:g.219925287G= | GRCh37 |
| NC_000002.10:g.219633531G= | NCBI36 |
| NG_016741.1:g.4952C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295731.7:c.-98C= MANE Select | ENSP00000295731.5:n.-98C= | |
| NM_002181.4:c.-98C= MANE Select | NP_002172.2:n.-98C= |