Linked Data
gnomAD v4:
2-112782579-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112782579A>T , CM000664.2:g.112782579A>T | GRCh38 |
| NC_000002.11:g.113540156A>T , CM000664.1:g.113540156A>T | GRCh37 |
| NC_000002.10:g.113256627A>T | NCBI36 |
| NG_008850.1:g.7816T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263339.4:c.96+137T>A MANE Select | ENSP00000263339.3:n.96+137T>A | |
| ENST00000263339.3:c.96+137T>A | ENSP00000263339.3:n.96+137T>A | |
| NM_000575.3:c.96+137T>A | NP_000566.3:n.96+137T>A | |
| NM_000575.4:c.96+137T>A | NP_000566.3:n.96+137T>A | |
| NM_000575.5:c.96+137T>A MANE Select | NP_000566.3:n.96+137T>A | |
| NM_001371554.1:c.96+137T>A | NP_001358483.1:n.96+137T>A |