Linked Data
gnomAD v4:
14-75008989-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75008989G>A , CM000676.2:g.75008989G>A | GRCh38 |
| NC_000014.8:g.75475692G>A , CM000676.1:g.75475692G>A | GRCh37 |
| NC_000014.7:g.74545445G>A | NCBI36 |
| NG_013333.1:g.11081G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.899-42G>A MANE Select | ENSP00000266126.5:n.899-42G>A | |
| ENST00000266126.9:c.899-42G>A | ENSP00000266126.5:n.899-42G>A | |
| ENST00000556668.1:n.479-42G>A | ||
| NM_014239.3:c.899-42G>A | NP_055054.1:n.899-42G>A | |
| NM_014239.4:c.899-42G>A MANE Select | NP_055054.1:n.899-42G>A |