Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.18026269G>C , CM000673.2:g.18026269G>C | GRCh38 |
| NC_000011.9:g.18047816G>C , CM000673.1:g.18047816G>C | GRCh37 |
| NC_000011.8:g.18004392G>C | NCBI36 |
| NG_011947.1:g.19520C>G | |
| NG_011947.2:g.19520C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004179.3:c.803+221C>G MANE Select | NP_004170.1:n.803+221C>G |
| ENST00000682019.1:c.803+221C>G MANE Select | ENSP00000508368.1:n.803+221C>G |
| NM_004179.2:c.803+221C>G | NP_004170.1:n.803+221C>G |
| ENST00000250018.6:c.803+221C>G | ENSP00000250018.2:n.803+221C>G |
| ENST00000417164.5:c.606+221C>G | ENSP00000403831.1:n.606+221C>G |