Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94000567C>T , CM000663.2:g.94000567C>T | GRCh38 |
| NC_000001.10:g.94466123C>T , CM000663.1:g.94466123C>T | GRCh37 |
| NC_000001.9:g.94238711C>T | NCBI36 |
| NG_009073.1:g.125583G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.6479+269G>A MANE Select | NP_000341.2:n.6479+269G>A |
| ENST00000370225.4:c.6479+269G>A MANE Select | ENSP00000359245.3:n.6479+269G>A |
| NM_000350.2:c.6479+269G>A | NP_000341.2:n.6479+269G>A |
| ENST00000370225.3:c.6479+269G>A | ENSP00000359245.3:n.6479+269G>A |
| ENST00000536513.5:c.2855+269G>A | ENSP00000439707.2:n.2855+269G>A |