Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31719317G= , CM000668.2:g.31719317G= | GRCh38 |
| NC_000006.11:g.31687094G= , CM000668.1:g.31687094G= | GRCh37 |
| NC_000006.10:g.31795073G= | NCBI36 |
| NG_029044.1:g.974G= | |
| NG_029044.2:g.974G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375819.3:c.164-7C= (LY6G6C) MANE Select | ENSP00000364978.2:n.164-7C= | |
| ENST00000375819.2:c.164-7C= (LY6G6C) | ENSP00000364978.2:n.164-7C= | |
| ENST00000460663.5:n.90+634G= (MPIG6B) | ||
| ENST00000495859.1:c.-5-7C= (LY6G6C) | ENSP00000433207.1:n.-5-7C= | |
| NM_025261.2:c.164-7C= (LY6G6C) | NP_079537.1:n.164-7C= | |
| NM_025261.3:c.164-7C= (LY6G6C) MANE Select | NP_079537.1:n.164-7C= |