Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152325202A= , CM000663.2:g.152325202A= | GRCh38 |
| NC_000001.10:g.152297678A= , CM000663.1:g.152297678A= | GRCh37 |
| NC_000001.9:g.150564302A= | NCBI36 |
| NG_016190.1:g.5002T= , LRG_1028:g.5002T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.-35T= MANE Select | ENSP00000357789.1:n.-35T= | |
| ENST00000368799.1:c.-35T= | ENSP00000357789.1:n.-35T= | |
| NM_002016.1:c.-35T= , LRG_1028t1:c.-35T= | NP_002007.1:n.-35T= | |
| NR_103778.1:n.915-7381A= | ||
| XM_011509329.1:c.-35T= | XP_011507631.1:n.-35T= | |
| NM_002016.2:c.-35T= MANE Select | NP_002007.1:n.-35T= |