Linked Data
gnomAD v4:
13-48045992-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045992T>A , CM000675.2:g.48045992T>A | GRCh38 |
| NC_000013.10:g.48620128T>A , CM000675.1:g.48620128T>A | GRCh37 |
| NC_000013.9:g.47518129T>A | NCBI36 |
| NG_047021.1:g.13426T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.*193T>A MANE Select | ENSP00000258662.1:n.*193T>A | |
| ENST00000258662.2:c.*193T>A | ENSP00000258662.1:n.*193T>A | |
| NM_018283.2:c.*193T>A | NP_060753.1:n.*193T>A | |
| NM_018283.3:c.*193T>A | NP_060753.1:n.*193T>A | |
| NR_136687.1:n.718+150T>A | ||
| NR_136688.1:n.675+193T>A | ||
| NM_018283.4:c.*193T>A MANE Select | NP_060753.1:n.*193T>A | |
| NR_136687.2:n.559+150T>A | ||
| NR_136688.2:n.516+193T>A |