Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142957803T>C , CM000669.2:g.142957803T>C | GRCh38 |
| NC_000007.13:g.142654890T>C , CM000669.1:g.142654890T>C | GRCh37 |
| NC_000007.12:g.142365012T>C | NCBI36 |
| NG_007492.1:g.9614A>G | |
| NG_007492.2:g.9614A>G | |
| NG_007492.3:g.9614A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355265.7:c.672+24A>G MANE Select | ENSP00000347409.2:n.672+24A>G | |
| ENST00000355265.6:c.672+24A>G | ENSP00000347409.2:n.672+24A>G | |
| ENST00000476829.5:c.525+501A>G | ENSP00000419889.1:n.525+501A>G | |
| ENST00000479768.6:n.790+24A>G | ||
| ENST00000494148.1:n.271+24A>G | ||
| NM_000420.2:c.672+24A>G | NP_000411.1:n.672+24A>G | |
| XM_005249993.2:c.708+24A>G | XP_005250050.1:n.708+24A>G | |
| NM_000420.3:c.672+24A>G MANE Select | NP_000411.1:n.672+24A>G |