Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19958727A>C , CM000670.2:g.19958727A>C | GRCh38 |
| NC_000008.10:g.19816238A>C , CM000670.1:g.19816238A>C | GRCh37 |
| NC_000008.9:g.19860518A>C | NCBI36 |
| NG_008855.1:g.24657A>C | |
| NG_008855.2:g.62011A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.1019-533A>C MANE Select | NP_000228.1:n.1019-533A>C |
| ENST00000650287.1:c.1019-533A>C MANE Select | ENSP00000497642.1:n.1019-533A>C |
| NM_000237.2:c.1019-533A>C | NP_000228.1:n.1019-533A>C |
| ENST00000311322.8:c.1019-533A>C | ENSP00000309757.6:n.1019-533A>C |
| ENST00000650478.1:c.80-2174A>C | ENSP00000497560.1:n.80-2174A>C |