Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.174764872T= , CM000664.2:g.174764872T= | GRCh38 |
| NC_000002.11:g.175629600T= , CM000664.1:g.175629600T= | GRCh37 |
| NC_000002.10:g.175337846T= | NCBI36 |
| NG_008172.1:g.4601A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000636168.2:c.-446-5239A= | ENSP00000490338.2:n.-446-5239A= |