Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37804995T= , CM000685.2:g.37804995T= | GRCh38 |
| NC_000023.10:g.37664248T= , CM000685.1:g.37664248T= | GRCh37 |
| NC_000023.9:g.37549192T= | NCBI36 |
| NG_009065.1:g.29979T= , LRG_53:g.29979T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.*661-11T= | ENSP00000512461.1:n.*661-11T= | |
| ENST00000696171.1:c.1056-11T= | ENSP00000512462.1:n.1056-11T= | |
| ENST00000378588.5:c.1152-11T= MANE Select | ENSP00000367851.4:n.1152-11T= | |
| ENST00000378588.4:c.1152-11T= | ENSP00000367851.4:n.1152-11T= | |
| ENST00000465127.1:c.171+378995T= | ENSP00000417050.1:n.171+378995T= | |
| NM_000397.3:c.1152-11T= , LRG_53t1:c.1152-11T= | NP_000388.2:n.1152-11T= | |
| XM_011543890.1:c.846-11T= | XP_011542192.1:n.846-11T= | |
| NM_000397.4:c.1152-11T= MANE Select | NP_000388.2:n.1152-11T= |