Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714381G= , CM000681.2:g.6714381G= | GRCh38 |
| NC_000019.9:g.6714392G= , CM000681.1:g.6714392G= | GRCh37 |
| NC_000019.8:g.6665392G= | NCBI36 |
| NG_009557.1:g.11271C= , LRG_27:g.11271C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.447C= | ENSP00000512083.1:p.Pro149= | |
| ENST00000245907.11:c.570C= MANE Select | ENSP00000245907.4:p.Pro190= | |
| ENST00000245907.10:c.570C= | ENSP00000245907.4:p.Pro190= | |
| NM_000064.3:c.570C= | NP_000055.2:p.Pro190= | |
| NM_000064.4:c.570C= MANE Select | NP_000055.2:p.Pro190= |