Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63942629T>G , CM000679.2:g.63942629T>G | GRCh38 |
| NC_000017.10:g.62019989T>G , CM000679.1:g.62019989T>G | GRCh37 |
| NC_000017.9:g.59373721T>G | NCBI36 |
| NG_011699.1:g.35290A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.4288+197A>C MANE Select | NP_000325.4:n.4288+197A>C |
| ENST00000435607.3:c.4288+197A>C MANE Select | ENSP00000396320.1:n.4288+197A>C |
| ENST00000578147.5:c.4288+197A>C | ENSP00000463963.1:n.4288+197A>C |
| XM_005257566.3:c.4288+197A>C | XP_005257623.1:n.4288+197A>C |