Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127814187C>A , CM000671.2:g.127814187C>A | GRCh38 |
| NC_000009.11:g.130576466C>A , CM000671.1:g.130576466C>A | GRCh37 |
| NC_000009.10:g.129616287C>A | NCBI36 |
| NG_009551.1:g.45582G>T , LRG_589:g.45582G>T | |
| NG_023245.1:g.16313C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000467826.5:n.710-21C>A | |
| XM_005251864.2:c.1484-21C>A | XP_005251921.1:n.1484-21C>A |
| XM_005251864.4:c.1484-21C>A | XP_005251921.1:n.1484-21C>A |
| XM_017014565.2:c.1334-21C>A | XP_016870054.1:n.1334-21C>A |
| XR_242582.2:n.1381-21C>A | |
| XR_242582.4:n.1379-21C>A |