Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208124113T= , CM000664.2:g.208124113T= | GRCh38 |
| NC_000002.11:g.208988837T= , CM000664.1:g.208988837T= | GRCh37 |
| NC_000002.10:g.208697082T= | NCBI36 |
| NG_008039.1:g.5477A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264376.5:c.251A= MANE Select | ENSP00000264376.4:p.His84= | |
| ENST00000264376.4:c.251A= | ENSP00000264376.4:p.His84= | |
| NM_006891.3:c.251A= | NP_008822.2:p.His84= | |
| NR_038437.1:n.97+4888T= | ||
| NM_006891.4:c.251A= MANE Select | NP_008822.2:p.His84= |