Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110169558T>C , CM000675.2:g.110169558T>C | GRCh38 |
| NC_000013.10:g.110821905T>C , CM000675.1:g.110821905T>C | GRCh37 |
| NC_000013.9:g.109619906T>C | NCBI36 |
| NG_011544.2:g.142592A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3876+71A>G MANE Select | ENSP00000364979.4:n.3876+71A>G | |
| ENST00000650424.1:c.32+71A>G | ||
| ENST00000375820.8:c.3876+71A>G | ENSP00000364979.4:n.3876+71A>G | |
| NM_001845.5:c.3876+71A>G | NP_001836.3:n.3876+71A>G | |
| XM_011521048.1:c.3684+71A>G | XP_011519350.1:n.3684+71A>G | |
| XM_011521048.2:c.3684+71A>G | XP_011519350.1:n.3684+71A>G | |
| NM_001845.6:c.3876+71A>G MANE Select | NP_001836.3:n.3876+71A>G |