Linked Data
gnomAD v4:
8-86739580-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739580C>T , CM000670.2:g.86739580C>T | GRCh38 |
| NC_000008.10:g.87751808C>T , CM000670.1:g.87751808C>T | GRCh37 |
| NC_000008.9:g.87820924C>T | NCBI36 |
| NG_016980.1:g.9096G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.211+75G>A MANE Select | ENSP00000316605.5:n.211+75G>A | |
| ENST00000681746.1:c.211+75G>A | ENSP00000505959.1:n.211+75G>A | |
| ENST00000320005.5:c.211+75G>A | ENSP00000316605.5:n.211+75G>A | |
| ENST00000519777.1:n.193+75G>A | ||
| NM_019098.4:c.211+75G>A | NP_061971.3:n.211+75G>A | |
| NM_019098.5:c.211+75G>A MANE Select | NP_061971.3:n.211+75G>A |