Linked Data
dbSNP Id:
rs780770660
gnomAD v4:
6-6588560-C-T
MyVariant Identifiers:
chr6:g.6588560C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588560C>T , CM000668.2:g.6588560C>T | GRCh38 |
| NC_000006.11:g.6588793C>T , CM000668.1:g.6588793C>T | GRCh37 |
| NC_000006.10:g.6533792C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379953.6:c.-10+110C>T (LY86) | ENSP00000369286.1:n.-10+110C>T | |
| NR_026970.1:n.196-19071G>A (LY86-AS1) |