Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31719232C= , CM000668.2:g.31719232C= | GRCh38 |
| NC_000006.11:g.31687009C= , CM000668.1:g.31687009C= | GRCh37 |
| NC_000006.10:g.31794988C= | NCBI36 |
| NG_029044.1:g.889C= | |
| NG_029044.2:g.889C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375819.3:c.242G= (LY6G6C) MANE Select | ENSP00000364978.2:p.Arg81= | |
| ENST00000375819.2:c.242G= (LY6G6C) | ENSP00000364978.2:p.Arg81= | |
| ENST00000460663.5:n.90+549C= (MPIG6B) | ||
| ENST00000495859.1:c.74G= (LY6G6C) | ENSP00000433207.1:p.Arg25= | |
| NM_025261.2:c.242G= (LY6G6C) | NP_079537.1:p.Arg81= | |
| NM_025261.3:c.242G= (LY6G6C) MANE Select | NP_079537.1:p.Arg81= |