Linked Data
gnomAD v4:
13-48045885-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045885C>T , CM000675.2:g.48045885C>T | GRCh38 |
| NC_000013.10:g.48620021C>T , CM000675.1:g.48620021C>T | GRCh37 |
| NC_000013.9:g.47518022C>T | NCBI36 |
| NG_047021.1:g.13319C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.*86C>T MANE Select | ENSP00000258662.1:n.*86C>T | |
| ENST00000258662.2:c.*86C>T | ENSP00000258662.1:n.*86C>T | |
| NM_018283.2:c.*86C>T | NP_060753.1:n.*86C>T | |
| NM_018283.3:c.*86C>T | NP_060753.1:n.*86C>T | |
| NR_136687.1:n.718+43C>T | ||
| NR_136688.1:n.675+86C>T | ||
| NM_018283.4:c.*86C>T MANE Select | NP_060753.1:n.*86C>T | |
| NR_136687.2:n.559+43C>T | ||
| NR_136688.2:n.516+86C>T |