Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75005946G>C , CM000676.2:g.75005946G>C | GRCh38 |
| NC_000014.8:g.75472649G>C , CM000676.1:g.75472649G>C | GRCh37 |
| NC_000014.7:g.74542402G>C | NCBI36 |
| NG_013333.1:g.8038G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.678G>C MANE Select | ENSP00000266126.5:p.Met226Ile | |
| ENST00000266126.9:c.678G>C | ENSP00000266126.5:p.Met226Ile | |
| ENST00000553401.5:c.676G>C | ENSP00000451681.1:n.676G>C | |
| ENST00000554748.2:c.42G>C | ENSP00000452582.2:p.Met14Ile | |
| ENST00000556028.5:c.*26G>C | ENSP00000452311.1:n.*26G>C | |
| NM_014239.3:c.678G>C | NP_055054.1:p.Met226Ile | |
| NM_014239.4:c.678G>C MANE Select | NP_055054.1:p.Met226Ile |