Linked Data
gnomAD v4:
11-637595-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.637595C>T , CM000673.2:g.637595C>T | GRCh38 |
| NC_000011.9:g.637595C>T , CM000673.1:g.637595C>T | GRCh37 |
| NC_000011.8:g.627595C>T | NCBI36 |
| NG_021241.1:g.5291C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000176183.6:c.285+6C>T MANE Select | ENSP00000176183.5:n.285+6C>T | |
| ENST00000176183.5:c.285+6C>T | ENSP00000176183.5:n.285+6C>T | |
| NM_000797.3:c.285+6C>T | NP_000788.2:n.285+6C>T | |
| NM_000797.4:c.285+6C>T MANE Select | NP_000788.2:n.285+6C>T |