Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21205999G>C , CM000674.2:g.21205999G>C | GRCh38 |
| NC_000012.11:g.21358933G>C , CM000674.1:g.21358933G>C | GRCh37 |
| NC_000012.10:g.21250200G>C | NCBI36 |
| NG_011745.1:g.79806G>C , LRG_1022:g.79806G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006446.5:c.1463G>C MANE Select | NP_006437.3:p.Gly488Ala |
| ENST00000256958.3:c.1463G>C MANE Select | ENSP00000256958.2:p.Gly488Ala |
| NM_006446.4:c.1463G>C , LRG_1022t1:c.1463G>C | NP_006437.3:p.Gly488Ala |
| ENST00000256958.2:c.1463G>C | ENSP00000256958.2:p.Gly488Ala |