Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94974606T>C , CM000672.2:g.94974606T>C | GRCh38 |
| NC_000010.10:g.96734363T>C , CM000672.1:g.96734363T>C | GRCh37 |
| NC_000010.9:g.96724353T>C | NCBI36 |
| NG_008385.1:g.40949T>C | |
| NG_008385.2:g.41449T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.961+2361T>C MANE Select | ENSP00000260682.6:n.961+2361T>C | |
| ENST00000643112.1:c.820-6577T>C | ENSP00000496202.1:n.820-6577T>C | |
| ENST00000260682.6:c.961+2361T>C | ENSP00000260682.6:n.961+2361T>C | |
| NM_000771.3:c.961+2361T>C | NP_000762.2:n.961+2361T>C | |
| NM_000771.4:c.961+2361T>C MANE Select | NP_000762.2:n.961+2361T>C |