Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29916983C>A , CM000664.2:g.29916983C>A | GRCh38 |
| NC_000002.11:g.30139849C>A , CM000664.1:g.30139849C>A | GRCh37 |
| NC_000002.10:g.29993353C>A | NCBI36 |
| NG_009445.1:g.9584G>T , LRG_488:g.9584G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.667+3010G>T MANE Select | ENSP00000373700.3:n.667+3010G>T | |
| ENST00000389048.7:c.667+3010G>T | ENSP00000373700.3:n.667+3010G>T | |
| NM_004304.4:c.667+3010G>T | NP_004295.2:n.667+3010G>T | |
| XR_001738688.2:n.1597+3010G>T | ||
| NM_004304.5:c.667+3010G>T MANE Select | NP_004295.2:n.667+3010G>T |