Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787711A>G , CM000681.2:g.18787711A>G | GRCh38 |
| NC_000019.9:g.18898520A>G , CM000681.1:g.18898520A>G | GRCh37 |
| NC_000019.8:g.18759520A>G | NCBI36 |
| NG_007070.1:g.8595T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.976-61T>C MANE Select | ENSP00000222271.2:n.976-61T>C | |
| ENST00000222271.6:c.976-61T>C | ENSP00000222271.2:n.976-61T>C | |
| ENST00000425807.1:c.817-61T>C | ENSP00000403792.1:n.817-61T>C | |
| ENST00000542601.6:c.877-61T>C | ENSP00000439156.2:n.877-61T>C | |
| NM_000095.2:c.976-61T>C | NP_000086.2:n.976-61T>C | |
| NM_000095.3:c.976-61T>C MANE Select | NP_000086.2:n.976-61T>C |