Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.96057343A= , CM000668.2:g.96057343A= | GRCh38 |
| NC_000006.11:g.96505219A= , CM000668.1:g.96505219A= | GRCh37 |
| NC_000006.10:g.96611940A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006581.4:c.-98+41131A= MANE Select | NP_006572.2:n.-98+41131A= |
| ENST00000302103.6:c.-98+41131A= MANE Select | ENSP00000302599.4:n.-98+41131A= |
| NM_006581.3:c.-98+41131A= | NP_006572.2:n.-98+41131A= |
| ENST00000302103.5:c.-98+41131A= | ENSP00000302599.4:n.-98+41131A= |
| XM_011535384.1:c.-98+36370A= | XP_011533686.1:n.-98+36370A= |
| XM_017010190.1:c.-215+41131A= | XP_016865679.1:n.-215+41131A= |
| XR_001744267.2:n.1915T= |