Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94036739C>T , CM000663.2:g.94036739C>T | GRCh38 |
| NC_000001.10:g.94502295C>T , CM000663.1:g.94502295C>T | GRCh37 |
| NC_000001.9:g.94274883C>T | NCBI36 |
| NG_009073.1:g.89411G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.3862+1G>A MANE Select | ENSP00000359245.3:n.3862+1G>A | |
| ENST00000370225.3:c.3862+1G>A | ENSP00000359245.3:n.3862+1G>A | |
| ENST00000536513.5:c.238+1G>A | ENSP00000439707.2:n.238+1G>A | |
| NM_000350.2:c.3862+1G>A | NP_000341.2:n.3862+1G>A | |
| NM_000350.3:c.3862+1G>A MANE Select | NP_000341.2:n.3862+1G>A |