Linked Data
gnomAD v4:
4-46123691-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46123691A>T , CM000666.2:g.46123691A>T | GRCh38 |
| NC_000004.11:g.46125708A>T , CM000666.1:g.46125708A>T | GRCh37 |
| NC_000004.10:g.45820465A>T | NCBI36 |
| NG_046964.1:g.5375T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295452.5:c.104+119T>A MANE Select | ENSP00000295452.4:n.104+119T>A | |
| ENST00000295452.4:c.104+119T>A | ENSP00000295452.4:n.104+119T>A | |
| NM_173536.3:c.104+119T>A | NP_775807.2:n.104+119T>A | |
| NM_173536.4:c.104+119T>A MANE Select | NP_775807.2:n.104+119T>A |