Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6695979A= , CM000666.2:g.6695979A= | GRCh38 |
| NC_000004.11:g.6697706A= , CM000666.1:g.6697706A= | GRCh37 |
| NC_000004.10:g.6748607A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296370.4:c.139-914A= MANE Select | ENSP00000296370.3:n.139-914A= | |
| ENST00000296370.3:c.139-914A= | ENSP00000296370.3:n.139-914A= | |
| ENST00000513778.1:n.36-914A= | ||
| NM_005980.2:c.139-914A= | NP_005971.1:n.139-914A= | |
| NM_005980.3:c.139-914A= MANE Select | NP_005971.1:n.139-914A= |