Linked Data
gnomAD v4:
15-43599494-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43599494G>C , CM000677.2:g.43599494G>C | GRCh38 |
| NC_000015.9:g.43891692G>C , CM000677.1:g.43891692G>C | GRCh37 |
| NC_000015.8:g.41678984G>C | NCBI36 |
| NG_011636.1:g.24307C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411560.1:n.103G>C (CKMT1B) | ||
| ENST00000450892.6:c.*178C>G (STRC) | ENSP00000401513.2:n.*178C>G | |
| XM_011521277.1:c.*178C>G (STRC) | XP_011519579.1:n.*178C>G | |
| XM_011521278.1:c.*178C>G (STRC) | XP_011519580.1:n.*178C>G | |
| XM_011521279.1:c.*178C>G (STRC) | XP_011519581.1:n.*178C>G |