Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154993330C= , CM000685.2:g.154993330C= | GRCh38 |
| NC_000023.10:g.154221605C= , CM000685.1:g.154221605C= | GRCh37 |
| NC_000023.9:g.153874799C= | NCBI36 |
| NG_011403.1:g.34394G= | |
| NG_011403.2:g.34394G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.389-182G= MANE Select | ENSP00000353393.4:n.389-182G= | |
| ENST00000647125.1:c.*175-182G= | ENSP00000496062.1:n.*175-182G= | |
| ENST00000360256.8:c.389-182G= | ENSP00000353393.4:n.389-182G= | |
| ENST00000423959.5:c.284-182G= | ENSP00000409446.1:n.284-182G= | |
| ENST00000453950.1:c.371-182G= | ENSP00000389153.1:n.371-182G= | |
| NM_000132.3:c.389-182G= | NP_000123.1:n.389-182G= | |
| XM_011531126.1:c.284-182G= | XP_011529428.1:n.284-182G= | |
| NM_000132.4:c.389-182G= MANE Select | NP_000123.1:n.389-182G= |