Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31125695T>C , CM000668.2:g.31125695T>C | GRCh38 |
| NC_000006.11:g.31093472T>C , CM000668.1:g.31093472T>C | GRCh37 |
| NC_000006.10:g.31201451T>C | NCBI36 |
| NG_021348.1:g.15865T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259881.10:c.-209T>C MANE Select | ENSP00000259881.9:n.-209T>C | |
| ENST00000259881.9:c.-209T>C | ENSP00000259881.9:n.-209T>C | |
| ENST00000479581.5:n.61+10804T>C | ||
| ENST00000548049.1:n.136T>C | ||
| ENST00000550838.1:n.59-44T>C | ||
| ENST00000552747.1:n.53+10804T>C | ||
| NM_014068.2:c.-209T>C | NP_054787.2:n.-209T>C | |
| NM_014068.3:c.-209T>C MANE Select | NP_054787.2:n.-209T>C |