Linked Data
gnomAD v4:
18-77268554-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268554T>C , CM000680.2:g.77268554T>C | GRCh38 |
| NC_000018.9:g.74980510T>C , CM000680.1:g.74980510T>C | GRCh37 |
| NC_000018.8:g.73109498T>C | NCBI36 |
| NG_009223.1:g.23503T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-31T>C MANE Select | ENSP00000299727.3:n.733-31T>C | |
| ENST00000299727.4:c.733-31T>C | ENSP00000299727.3:n.733-31T>C | |
| NM_001480.3:c.733-31T>C | NP_001471.2:n.733-31T>C | |
| NM_001480.4:c.733-31T>C MANE Select | NP_001471.2:n.733-31T>C |