Linked Data
MyVariant Identifiers:
chr6:g.6589018C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588785C>T , CM000668.2:g.6588785C>T | GRCh38 |
| NC_000006.11:g.6589018C>T , CM000668.1:g.6589018C>T | GRCh37 |
| NC_000006.10:g.6534017C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230568.5:c.51C>T (LY86) MANE Select | ENSP00000230568.3:p.Ser17= | |
| ENST00000230568.4:c.51C>T (LY86) | ENSP00000230568.3:p.Ser17= | |
| ENST00000379953.6:c.51C>T (LY86) | ENSP00000369286.1:p.Ser17= | |
| NM_004271.3:c.51C>T (LY86) | NP_004262.1:p.Ser17= | |
| NR_026970.1:n.196-19296G>A (LY86-AS1) | ||
| XM_017011505.1:c.51C>T (LY86) | XP_016866994.1:p.Ser17= | |
| NM_004271.4:c.51C>T (LY86) MANE Select | NP_004262.1:p.Ser17= |