Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171651988C>G , CM000663.2:g.171651988C>G | GRCh38 |
| NC_000001.10:g.171621128C>G , CM000663.1:g.171621128C>G | GRCh37 |
| NC_000001.9:g.169887751C>G | NCBI36 |
| NG_008859.1:g.5646G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.604+20G>C MANE Select | ENSP00000037502.5:n.604+20G>C | |
| ENST00000638471.1:c.130+494G>C | ENSP00000491206.1:n.130+494G>C | |
| ENST00000037502.10:c.604+20G>C | ENSP00000037502.5:n.604+20G>C | |
| ENST00000614688.1:c.604+20G>C | ENSP00000478680.1:n.604+20G>C | |
| NM_000261.1:c.604+20G>C | NP_000252.1:n.604+20G>C | |
| NM_000261.2:c.604+20G>C MANE Select | NP_000252.1:n.604+20G>C |