Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43077066T>A , CM000672.2:g.43077066T>A | GRCh38 |
| NC_000010.10:g.43572514T>A , CM000672.1:g.43572514T>A | GRCh37 |
| NC_000010.9:g.42892520T>A | NCBI36 |
| NG_007489.1:g.4998T>A , LRG_518:g.4998T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000671844.1:c.-193T>A | ENSP00000500541.1:n.-193T>A | |
| ENST00000355710.7:c.-193T>A | ENSP00000347942.3:n.-193T>A | |
| XM_011540027.1:c.-193T>A | XP_011538329.1:n.-193T>A | |
| NM_020630.5:c.-193T>A | NP_065681.1:n.-193T>A | |
| NM_020975.5:c.-193T>A | NP_066124.1:n.-193T>A |