Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232540715A>G , CM000664.2:g.232540715A>G | GRCh38 |
| NC_000002.11:g.233405425A>G , CM000664.1:g.233405425A>G | GRCh37 |
| NC_000002.10:g.233113669A>G | NCBI36 |
| NG_012954.1:g.5989A>G | |
| NG_012954.2:g.6024A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005199.5:c.350+4A>G MANE Select | NP_005190.4:n.350+4A>G |
| ENST00000651502.1:c.350+4A>G MANE Select | ENSP00000498757.1:n.350+4A>G |
| NM_005199.4:c.350+4A>G | NP_005190.4:n.350+4A>G |
| ENST00000389492.3:c.350+4A>G | ENSP00000374143.3:n.350+4A>G |
| ENST00000389494.7:c.350+4A>G | ENSP00000374145.3:n.350+4A>G |
| ENST00000485094.1:n.371+4A>G |