Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.23522303G>C , CM000667.2:g.23522303G>C | GRCh38 |
| NC_000005.9:g.23522412G>C , CM000667.1:g.23522412G>C | GRCh37 |
| NC_000005.8:g.23558169G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502755.6:c.509-1G>C | ENSP00000425471.2:n.509-1G>C | |
| ENST00000296682.4:c.509-1G>C MANE Select | ENSP00000296682.4:n.509-1G>C | |
| ENST00000296682.3:c.509-1G>C | ENSP00000296682.3:n.509-1G>C | |
| ENST00000635252.1:c.332-1G>C | ENSP00000489227.1:n.332-1G>C | |
| NM_020227.2:c.509-1G>C | NP_064612.2:n.509-1G>C | |
| NM_020227.3:c.509-1G>C | NP_064612.2:n.509-1G>C | |
| NM_001376900.1:c.509-1G>C | NP_001363829.1:n.509-1G>C | |
| NM_020227.4:c.509-1G>C MANE Select | NP_064612.2:n.509-1G>C |