Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98874276A= , CM000668.2:g.98874276A= | GRCh38 |
| NC_000006.11:g.99322152A= , CM000668.1:g.99322152A= | GRCh37 |
| NC_000006.10:g.99428873A= | NCBI36 |
| NG_033903.1:g.78731T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369244.7:c.*2T= MANE Select | ENSP00000358247.1:n.*2T= | |
| ENST00000229971.2:c.*2T= | ENSP00000229971.1:n.*2T= | |
| ENST00000369244.6:c.*2T= | ENSP00000358247.1:n.*2T= | |
| NM_001278716.1:c.*2T= | NP_001265645.1:n.*2T= | |
| NM_012160.4:c.*2T= | NP_036292.2:n.*2T= | |
| NR_103836.1:n.1913T= | ||
| XM_005266930.1:c.*2T= | XP_005266987.1:n.*2T= | |
| XM_005266930.3:c.*2T= | XP_005266987.1:n.*2T= | |
| XM_017010726.1:c.*2T= | XP_016866215.1:n.*2T= | |
| XM_017010727.2:c.*2T= | XP_016866216.1:n.*2T= | |
| XM_017010728.1:c.*2T= | XP_016866217.1:n.*2T= | |
| NM_001278716.2:c.*2T= MANE Select | NP_001265645.1:n.*2T= | |
| NR_103836.2:n.1853T= | ||
| NM_012160.5:c.*2T= | NP_036292.2:n.*2T= |