Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63939702C>T , CM000679.2:g.63939702C>T | GRCh38 |
| NC_000017.10:g.62017062C>T , CM000679.1:g.62017062C>T | GRCh37 |
| NC_000017.9:g.59370794C>T | NCBI36 |
| NG_011699.1:g.38217G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.*1069G>A MANE Select | ENSP00000396320.1:n.*1069G>A | |
| ENST00000578147.5:c.*1069G>A | ENSP00000463963.1:n.*1069G>A | |
| NM_000334.4:c.*1069G>A MANE Select | NP_000325.4:n.*1069G>A | |
| XM_005257566.3:c.*1069G>A | XP_005257623.1:n.*1069G>A |