Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6709991A= , CM000681.2:g.6709991A= | GRCh38 |
| NC_000019.9:g.6710002A= , CM000681.1:g.6710002A= | GRCh37 |
| NC_000019.8:g.6661002A= | NCBI36 |
| NG_009557.1:g.15661T= , LRG_27:g.15661T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.1564-149T= | ENSP00000512083.1:n.1564-149T= | |
| ENST00000695654.1:c.811-149T= | ENSP00000512085.1:n.811-149T= | |
| ENST00000695655.1:c.592-113T= | ENSP00000512086.1:n.592-113T= | |
| ENST00000695692.1:n.1051-149T= | ||
| ENST00000245907.11:c.1687-149T= MANE Select | ENSP00000245907.4:n.1687-149T= | |
| ENST00000245907.10:c.1687-149T= | ENSP00000245907.4:n.1687-149T= | |
| ENST00000600763.1:n.320-149T= | ||
| NM_000064.3:c.1687-149T= | NP_000055.2:n.1687-149T= | |
| NM_000064.4:c.1687-149T= MANE Select | NP_000055.2:n.1687-149T= |