Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110169553A= , CM000675.2:g.110169553A= | GRCh38 |
| NC_000013.10:g.110821900A= , CM000675.1:g.110821900A= | GRCh37 |
| NC_000013.9:g.109619901A= | NCBI36 |
| NG_011544.2:g.142597T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3876+76T= MANE Select | ENSP00000364979.4:n.3876+76T= | |
| ENST00000650424.1:c.32+76T= | ||
| ENST00000375820.8:c.3876+76T= | ENSP00000364979.4:n.3876+76T= | |
| NM_001845.5:c.3876+76T= | NP_001836.3:n.3876+76T= | |
| XM_011521048.1:c.3684+76T= | XP_011519350.1:n.3684+76T= | |
| XM_011521048.2:c.3684+76T= | XP_011519350.1:n.3684+76T= | |
| NM_001845.6:c.3876+76T= MANE Select | NP_001836.3:n.3876+76T= |