Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827884G>C , CM000667.2:g.148827884G>C | GRCh38 |
| NC_000005.9:g.148207447G>C , CM000667.1:g.148207447G>C | GRCh37 |
| NC_000005.8:g.148187640G>C | NCBI36 |
| NG_016421.1:g.6292G>C | |
| NG_016421.2:g.6292G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000024.6:c.1053G>C MANE Select | NP_000015.2:p.Gly351= |
| ENST00000305988.6:c.1053G>C MANE Select | ENSP00000305372.4:p.Gly351= |
| NM_000024.5:c.1053G>C | NP_000015.1:p.Gly351= |
| ENST00000305988.5:c.1053G>C | ENSP00000305372.4:p.Gly351= |