Linked Data
MyVariant Identifiers:
chr6:g.31686993T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31719216T>C , CM000668.2:g.31719216T>C | GRCh38 |
| NC_000006.11:g.31686993T>C , CM000668.1:g.31686993T>C | GRCh37 |
| NC_000006.10:g.31794972T>C | NCBI36 |
| NG_029044.1:g.873T>C | |
| NG_029044.2:g.873T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375819.3:c.258A>G (LY6G6C) MANE Select | ENSP00000364978.2:p.Thr86= | |
| ENST00000375819.2:c.258A>G (LY6G6C) | ENSP00000364978.2:p.Thr86= | |
| ENST00000460663.5:n.90+533T>C (MPIG6B) | ||
| ENST00000495859.1:c.90A>G (LY6G6C) | ENSP00000433207.1:p.Thr30= | |
| NM_025261.2:c.258A>G (LY6G6C) | NP_079537.1:p.Thr86= | |
| NM_025261.3:c.258A>G (LY6G6C) MANE Select | NP_079537.1:p.Thr86= |