Linked Data
gnomAD v4:
14-60644851-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60644851C>A , CM000676.2:g.60644851C>A | GRCh38 |
| NC_000014.8:g.61111569C>A , CM000676.1:g.61111569C>A | GRCh37 |
| NC_000014.7:g.60181322C>A | NCBI36 |
| NG_008231.1:g.9587G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645694.3:c.*1432G>T MANE Select | ENSP00000494686.1:n.*1432G>T | |
| ENST00000247182.6:c.*1432G>T | ENSP00000247182.5:n.*1432G>T | |
| ENST00000554986.2:c.*1432G>T | ENSP00000452700.2:n.*1432G>T | |
| NM_005982.3:c.*1432G>T | NP_005973.1:n.*1432G>T | |
| XM_017021602.2:c.*1706G>T | XP_016877091.1:n.*1706G>T | |
| NM_005982.4:c.*1432G>T MANE Select | NP_005973.1:n.*1432G>T |