Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186197681T>A , CM000666.2:g.186197681T>A | GRCh38 |
| NC_000004.11:g.187118835T>A , CM000666.1:g.187118835T>A | GRCh37 |
| NC_000004.10:g.187355829T>A | NCBI36 |
| NG_007965.1:g.11162T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.674+79T>A MANE Select | ENSP00000368079.4:n.674+79T>A | |
| ENST00000378802.4:c.674+79T>A | ENSP00000368079.4:n.674+79T>A | |
| ENST00000507209.5:n.1515+79T>A | ||
| NM_207352.3:c.674+79T>A | NP_997235.3:n.674+79T>A | |
| XM_005262935.2:c.674+79T>A | XP_005262992.1:n.674+79T>A | |
| XM_006714184.2:c.278+79T>A | XP_006714247.1:n.278+79T>A | |
| XM_005262935.4:c.674+79T>A | XP_005262992.1:n.674+79T>A | |
| XM_017008037.1:c.278+79T>A | XP_016863526.1:n.278+79T>A | |
| NM_207352.4:c.674+79T>A MANE Select | NP_997235.3:n.674+79T>A |