Linked Data
gnomAD v4:
8-23682781-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23682781C>T , CM000670.2:g.23682781C>T | GRCh38 |
| NC_000008.10:g.23540294C>T , CM000670.1:g.23540294C>T | GRCh37 |
| NC_000008.9:g.23596239C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380871.5:c.109G>A MANE Select | ENSP00000370253.4:p.Asp37Asn | |
| ENST00000380871.4:c.109G>A | ENSP00000370253.4:p.Asp37Asn | |
| ENST00000523261.1:c.33+76G>A | ENSP00000429729.1:n.33+76G>A | |
| NM_001256339.1:c.33+76G>A | NP_001243268.1:n.33+76G>A | |
| NM_006167.3:c.109G>A | NP_006158.2:p.Asp37Asn | |
| NR_046072.1:n.18+123G>A | ||
| XR_001745842.1:n.1312+14031C>T | ||
| NM_006167.4:c.109G>A MANE Select | NP_006158.2:p.Asp37Asn | |
| NR_046072.2:n.35+123G>A |