Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23417705C= , CM000676.2:g.23417705C= | GRCh38 |
| NC_000014.8:g.23886914C= , CM000676.1:g.23886914C= | GRCh37 |
| NC_000014.7:g.22956754C= | NCBI36 |
| NG_007884.1:g.22957G= , LRG_384:g.22957G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.4170-19G= MANE Select | ENSP00000347507.3:n.4170-19G= | |
| ENST00000355349.3:c.4170-19G= | ENSP00000347507.3:n.4170-19G= | |
| NM_000257.3:c.4170-19G= | NP_000248.2:n.4170-19G= | |
| XM_017021340.1:c.4170-19G= | XP_016876829.1:n.4170-19G= | |
| NM_000257.4:c.4170-19G= MANE Select | NP_000248.2:n.4170-19G= |