MyVariant.info:
GRCh37
chr10:g.88730312T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.86970555T>A , CM000672.2:g.86970555T>A | GRCh38 |
| NC_000010.10:g.88730312T>A , CM000672.1:g.88730312T>A | GRCh37 |
| NC_000010.9:g.88720292T>A | NCBI36 |
| NG_032913.2:g.3927A>T | |
| NG_032913.3:g.3927A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372013.8:c.204T>A (ADIRF) MANE Select | ENSP00000361083.3:p.Ile68= | |
| ENST00000372013.7:c.204T>A (ADIRF) | ENSP00000361083.3:p.Ile68= | |
| ENST00000561504.1:c.204T>A (ADIRF) | ENSP00000475582.1:p.Ile68= | |
| NM_006829.2:c.204T>A (ADIRF) | NP_006820.1:p.Ile68= | |
| NM_006829.3:c.204T>A (ADIRF) MANE Select | NP_006820.1:p.Ile68= | |
| NM_133447.2:c.-1390T>A (AGAP11) | NP_597704.1:n.-1390T>A | |
| NR_170177.1:n.237A>T (ADIRF-AS1) | ||
| NR_170178.1:n.203A>T (ADIRF-AS1) | ||
| NR_170179.1:n.237A>T (ADIRF-AS1) | ||
| NR_170180.1:n.237A>T (ADIRF-AS1) | ||
| NR_170181.1:n.237A>T (ADIRF-AS1) | ||
| NR_170182.1:n.237A>T (ADIRF-AS1) | ||
| NR_170183.1:n.686A>T (ADIRF-AS1) | ||
| NR_170184.1:n.686A>T (ADIRF-AS1) | ||
| NR_170185.1:n.686A>T (ADIRF-AS1) | ||
| NR_171046.1:n.220T>A (AGAP11) |