Linked Data
gnomAD v4:
6-6588690-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588690T>A , CM000668.2:g.6588690T>A | GRCh38 |
| NC_000006.11:g.6588923T>A , CM000668.1:g.6588923T>A | GRCh37 |
| NC_000006.10:g.6533922T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230568.4:c.-45T>A (LY86) | ENSP00000230568.3:n.-45T>A | |
| ENST00000379953.6:c.-9-36T>A (LY86) | ENSP00000369286.1:n.-9-36T>A | |
| NR_026970.1:n.196-19201A>T (LY86-AS1) | ||
| XM_017011505.1:c.-45T>A (LY86) | XP_016866994.1:n.-45T>A |