Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44379681G>C , CM000679.2:g.44379681G>C | GRCh38 |
| NC_000017.10:g.42457049G>C , CM000679.1:g.42457049G>C | GRCh37 |
| NC_000017.9:g.39812575G>C | NCBI36 |
| NG_008331.1:g.14825C>G , LRG_479:g.14825C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262407.6:c.1878+8C>G MANE Select | ENSP00000262407.5:n.1878+8C>G | |
| ENST00000648408.1:c.1309+8C>G | ||
| ENST00000262407.5:c.1878+8C>G | ENSP00000262407.5:n.1878+8C>G | |
| ENST00000592462.5:n.673+8C>G | ||
| NM_000419.3:c.1878+8C>G , LRG_479t1:c.1878+8C>G | NP_000410.2:n.1878+8C>G | |
| XM_011524749.1:c.1878+8C>G | XP_011523051.1:n.1878+8C>G | |
| XM_011524750.1:c.1878+8C>G | XP_011523052.1:n.1878+8C>G | |
| NM_000419.4:c.1878+8C>G | NP_000410.2:n.1878+8C>G | |
| NM_000419.5:c.1878+8C>G MANE Select | NP_000410.2:n.1878+8C>G |