Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.109097655T>C , CM000670.2:g.109097655T>C | GRCh38 |
| NC_000008.10:g.110109884T>C , CM000670.1:g.110109884T>C | GRCh37 |
| NC_000008.9:g.110179060T>C | NCBI36 |
| NG_017161.1:g.15209T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518632.2:c.789+9354T>C MANE Select | ENSP00000430711.2:n.789+9354T>C | |
| ENST00000311762.2:c.789+9354T>C | ENSP00000309818.2:n.789+9354T>C | |
| ENST00000518632.1:c.789+9354T>C | ENSP00000430711.1:n.789+9354T>C | |
| NM_003301.5:c.789+9354T>C | NP_003292.1:n.789+9354T>C | |
| XM_011517263.1:c.789+9354T>C | XP_011515565.1:n.789+9354T>C | |
| XM_011517263.2:c.789+9354T>C | XP_011515565.1:n.789+9354T>C | |
| NM_003301.7:c.789+9354T>C MANE Select | NP_003292.1:n.789+9354T>C |