Linked Data
gnomAD v4:
13-110169540-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110169540A>G , CM000675.2:g.110169540A>G | GRCh38 |
| NC_000013.10:g.110821887A>G , CM000675.1:g.110821887A>G | GRCh37 |
| NC_000013.9:g.109619888A>G | NCBI36 |
| NG_011544.2:g.142610T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3876+89T>C MANE Select | ENSP00000364979.4:n.3876+89T>C | |
| ENST00000650424.1:c.32+89T>C | ||
| ENST00000375820.8:c.3876+89T>C | ENSP00000364979.4:n.3876+89T>C | |
| NM_001845.5:c.3876+89T>C | NP_001836.3:n.3876+89T>C | |
| XM_011521048.1:c.3684+89T>C | XP_011519350.1:n.3684+89T>C | |
| XM_011521048.2:c.3684+89T>C | XP_011519350.1:n.3684+89T>C | |
| NM_001845.6:c.3876+89T>C MANE Select | NP_001836.3:n.3876+89T>C |