Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31524626A= , CM000680.2:g.31524626A= | GRCh38 |
| NC_000018.9:g.29104589A= , CM000680.1:g.29104589A= | GRCh37 |
| NC_000018.8:g.27358587A= | NCBI36 |
| NG_007072.3:g.31385A= , LRG_397:g.31385A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682087.2:n.659+41A= | ||
| ENST00000683614.2:n.659+41A= | ||
| ENST00000682087.1:c.659+41A= | ||
| ENST00000683614.1:c.659+41A= | ||
| ENST00000261590.13:c.828+41A= MANE Select | ENSP00000261590.8:n.828+41A= | |
| ENST00000261590.12:c.828+41A= | ENSP00000261590.8:n.828+41A= | |
| NM_001943.3:c.828+41A= , LRG_397t1:c.828+41A= | NP_001934.2:n.828+41A= | |
| NM_001943.4:c.828+41A= | NP_001934.2:n.828+41A= | |
| XM_024451095.1:c.294+41A= | XP_024306863.1:n.294+41A= | |
| NM_001943.5:c.828+41A= MANE Select | NP_001934.2:n.828+41A= |