Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.42353677T>C , CM000681.2:g.42353677T>C | GRCh38 |
| NC_000019.9:g.42857829T>C , CM000681.1:g.42857829T>C | GRCh37 |
| NC_000019.8:g.47549669T>C | NCBI36 |
| NG_033030.1:g.33069T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001271938.2:c.3761+2T>C MANE Select | NP_001258867.1:n.3761+2T>C |
| ENST00000251268.11:c.3761+2T>C MANE Select | ENSP00000251268.5:n.3761+2T>C |
| NM_001271938.1:c.3761+2T>C | NP_001258867.1:n.3761+2T>C |
| NM_001410.2:c.3560+2T>C | NP_001401.2:n.3560+2T>C |
| NM_001410.3:c.3560+2T>C | NP_001401.2:n.3560+2T>C |
| ENST00000251268.10:c.3761+2T>C | ENSP00000251268.5:n.3761+2T>C |
| ENST00000334370.8:c.3560+2T>C | ENSP00000334219.4:n.3560+2T>C |
| ENST00000378073.5:c.-3325+2T>C | ENSP00000367313.4:n.-3325+2T>C |