Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114709528T= , CM000663.2:g.114709528T= | GRCh38 |
| NC_000001.10:g.115252149T= , CM000663.1:g.115252149T= | GRCh37 |
| NC_000001.9:g.115053672T= | NCBI36 |
| NG_007572.1:g.12367A= , LRG_92:g.12367A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.450+41A= MANE Select | ENSP00000358548.4:n.450+41A= | |
| ENST00000369535.4:c.450+41A= | ENSP00000358548.4:n.450+41A= | |
| NM_002524.4:c.450+41A= | NP_002515.1:n.450+41A= | |
| NM_002524.5:c.450+41A= MANE Select | NP_002515.1:n.450+41A= |