Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154996970C= , CM000685.2:g.154996970C= | GRCh38 |
| NC_000023.10:g.154225245C= , CM000685.1:g.154225245C= | GRCh37 |
| NC_000023.9:g.153878439C= | NCBI36 |
| NG_011403.1:g.30754G= | |
| NG_011403.2:g.30754G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.388+3G= MANE Select | ENSP00000353393.4:n.388+3G= | |
| ENST00000647125.1:c.*174+3G= | ENSP00000496062.1:n.*174+3G= | |
| ENST00000360256.8:c.388+3G= | ENSP00000353393.4:n.388+3G= | |
| ENST00000423959.5:c.283+3G= | ENSP00000409446.1:n.283+3G= | |
| ENST00000453950.1:c.370+3G= | ENSP00000389153.1:n.370+3G= | |
| NM_000132.3:c.388+3G= | NP_000123.1:n.388+3G= | |
| XM_011531126.1:c.283+3G= | XP_011529428.1:n.283+3G= | |
| NM_000132.4:c.388+3G= MANE Select | NP_000123.1:n.388+3G= |