Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189058982T>A , CM000664.2:g.189058982T>A | GRCh38 |
| NC_000002.11:g.189923708T>A , CM000664.1:g.189923708T>A | GRCh37 |
| NC_000002.10:g.189631953T>A | NCBI36 |
| NG_011799.1:g.125898A>T | |
| NG_011799.2:g.125898A>T | |
| NG_011799.3:g.171320A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2086-89A>T MANE Select | ENSP00000364000.3:n.2086-89A>T | |
| ENST00000374866.7:c.2086-89A>T | ENSP00000364000.3:n.2086-89A>T | |
| ENST00000470524.2:n.192-89A>T | ||
| ENST00000618828.1:c.925-89A>T | ENSP00000482184.1:n.925-89A>T | |
| NM_000393.3:c.2086-89A>T | NP_000384.2:n.2086-89A>T | |
| XM_011510573.1:c.1948-89A>T | XP_011508875.1:n.1948-89A>T | |
| NM_000393.4:c.2086-89A>T | NP_000384.2:n.2086-89A>T | |
| XM_011510573.3:c.1948-89A>T | XP_011508875.1:n.1948-89A>T | |
| NM_000393.5:c.2086-89A>T MANE Select | NP_000384.2:n.2086-89A>T |