Linked Data
gnomAD v4:
14-22843200-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.22843200C>A , CM000676.2:g.22843200C>A | GRCh38 |
| NC_000014.8:g.23312409C>A , CM000676.1:g.23312409C>A | GRCh37 |
| NC_000014.7:g.22382249C>A | NCBI36 |
| NG_046989.1:g.11668C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311852.11:c.689-57C>A MANE Select | ENSP00000308208.6:n.689-57C>A | |
| ENST00000548162.2:c.689-57C>A | ENSP00000506068.1:n.689-57C>A | |
| ENST00000680097.1:c.*4-57C>A | ENSP00000506631.1:n.*4-57C>A | |
| ENST00000680941.1:c.*86+28C>A | ENSP00000506378.1:n.*86+28C>A | |
| ENST00000311852.10:c.689-57C>A | ENSP00000308208.6:n.689-57C>A | |
| ENST00000548162.1:n.931-57C>A | ||
| NM_004995.3:c.689-57C>A | NP_004986.1:n.689-57C>A | |
| NM_004995.4:c.689-57C>A MANE Select | NP_004986.1:n.689-57C>A |