Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134491434A>G , CM000685.2:g.134491434A>G | GRCh38 |
| NC_000023.10:g.133625464A>G , CM000685.1:g.133625464A>G | GRCh37 |
| NC_000023.9:g.133453130A>G | NCBI36 |
| NG_012329.1:g.36290A>G | |
| NG_012329.2:g.36290A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000194.3:c.402+1229A>G MANE Select | NP_000185.1:n.402+1229A>G |
| ENST00000298556.8:c.402+1229A>G MANE Select | ENSP00000298556.7:n.402+1229A>G |
| NM_000194.2:c.402+1229A>G | NP_000185.1:n.402+1229A>G |
| ENST00000298556.7:c.402+1229A>G | ENSP00000298556.7:n.402+1229A>G |
| ENST00000462974.5:n.560+1229A>G | |
| ENST00000475720.1:n.360+1229A>G | |
| XM_011531328.1:c.420+1229A>G | XP_011529630.1:n.420+1229A>G |