Linked Data
gnomAD v4:
8-81478596-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478596C>T , CM000670.2:g.81478596C>T | GRCh38 |
| NC_000008.10:g.82390831C>T , CM000670.1:g.82390831C>T | GRCh37 |
| NC_000008.9:g.82553386C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*269G>A MANE Select | ENSP00000256104.4:n.*269G>A | |
| ENST00000256104.4:c.*269G>A | ENSP00000256104.4:n.*269G>A | |
| NM_001442.2:c.*269G>A | NP_001433.1:n.*269G>A | |
| XR_001745980.1:n.514+16622C>T | ||
| NM_001442.3:c.*269G>A MANE Select | NP_001433.1:n.*269G>A |