Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714011C= , CM000681.2:g.6714011C= | GRCh38 |
| NC_000019.9:g.6714022C= , CM000681.1:g.6714022C= | GRCh37 |
| NC_000019.8:g.6665022C= | NCBI36 |
| NG_009557.1:g.11641G= , LRG_27:g.11641G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.631G= | ENSP00000512083.1:p.Glu211= | |
| ENST00000245907.11:c.754G= MANE Select | ENSP00000245907.4:p.Glu252= | |
| ENST00000245907.10:c.754G= | ENSP00000245907.4:p.Glu252= | |
| ENST00000595577.1:n.258G= | ||
| NM_000064.3:c.754G= | NP_000055.2:p.Glu252= | |
| NM_000064.4:c.754G= MANE Select | NP_000055.2:p.Glu252= |