Linked Data
MyVariant Identifiers:
chr6:g.31687014G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31719237G>A , CM000668.2:g.31719237G>A | GRCh38 |
| NC_000006.11:g.31687014G>A , CM000668.1:g.31687014G>A | GRCh37 |
| NC_000006.10:g.31794993G>A | NCBI36 |
| NG_029044.1:g.894G>A | |
| NG_029044.2:g.894G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375819.3:c.237C>T (LY6G6C) MANE Select | ENSP00000364978.2:p.Thr79= | |
| ENST00000375819.2:c.237C>T (LY6G6C) | ENSP00000364978.2:p.Thr79= | |
| ENST00000460663.5:n.90+554G>A (MPIG6B) | ||
| ENST00000495859.1:c.69C>T (LY6G6C) | ENSP00000433207.1:p.Thr23= | |
| NM_025261.2:c.237C>T (LY6G6C) | NP_079537.1:p.Thr79= | |
| NM_025261.3:c.237C>T (LY6G6C) MANE Select | NP_079537.1:p.Thr79= |