Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111622C>T , CM000670.2:g.118111622C>T | GRCh38 |
| NC_000008.10:g.119123861C>T , CM000670.1:g.119123861C>T | GRCh37 |
| NC_000008.9:g.119193042C>T | NCBI36 |
| NG_007455.2:g.5198G>A , LRG_493:g.5198G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-576G>A MANE Select | ENSP00000367446.3:n.-576G>A | |
| ENST00000378204.6:c.-576G>A | ENSP00000367446.2:n.-576G>A | |
| NM_000127.2:c.-576G>A , LRG_493t1:c.-576G>A | NP_000118.2:n.-576G>A | |
| NM_000127.3:c.-576G>A MANE Select | NP_000118.2:n.-576G>A |