Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714208G= , CM000681.2:g.6714208G= | GRCh38 |
| NC_000019.9:g.6714219G= , CM000681.1:g.6714219G= | GRCh37 |
| NC_000019.8:g.6665219G= | NCBI36 |
| NG_009557.1:g.11444C= , LRG_27:g.11444C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000064.4:c.640C= MANE Select | NP_000055.2:p.Pro214= |
| ENST00000245907.11:c.640C= MANE Select | ENSP00000245907.4:p.Pro214= |
| NM_000064.3:c.640C= | NP_000055.2:p.Pro214= |
| ENST00000245907.10:c.640C= | ENSP00000245907.4:p.Pro214= |
| ENST00000595577.1:n.144C= | |
| ENST00000695652.1:c.517C= | ENSP00000512083.1:p.Pro173= |