Linked Data
gnomAD v4:
6-6588567-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588567C>T , CM000668.2:g.6588567C>T | GRCh38 |
| NC_000006.11:g.6588800C>T , CM000668.1:g.6588800C>T | GRCh37 |
| NC_000006.10:g.6533799C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379953.6:c.-10+117C>T (LY86) | ENSP00000369286.1:n.-10+117C>T | |
| NR_026970.1:n.196-19078G>A (LY86-AS1) |