Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6167422T>C , CM000668.2:g.6167422T>C | GRCh38 |
| NC_000006.11:g.6167655T>C , CM000668.1:g.6167655T>C | GRCh37 |
| NC_000006.10:g.6112654T>C | NCBI36 |
| NG_008107.1:g.158270A>G , LRG_549:g.158270A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.1908+36A>G MANE Select | ENSP00000264870.3:n.1908+36A>G | |
| ENST00000264870.7:c.1908+36A>G | ENSP00000264870.3:n.1908+36A>G | |
| NM_000129.3:c.1908+36A>G , LRG_549t1:c.1908+36A>G | NP_000120.2:n.1908+36A>G | |
| XM_006715010.2:c.1908+36A>G | XP_006715073.1:n.1908+36A>G | |
| XM_011514342.1:c.2070+36A>G | XP_011512644.1:n.2070+36A>G | |
| NM_000129.4:c.1908+36A>G MANE Select | NP_000120.2:n.1908+36A>G |