Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49130919A= , CM000665.2:g.49130919A= | GRCh38 |
| NC_000003.11:g.49168352A= , CM000665.1:g.49168352A= | GRCh37 |
| NC_000003.10:g.49143356A= | NCBI36 |
| NG_008094.1:g.7248T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.915+31T= MANE Select | ENSP00000307156.4:n.915+31T= | |
| ENST00000305544.8:c.915+31T= | ENSP00000307156.4:n.915+31T= | |
| ENST00000418109.5:c.915+31T= | ENSP00000388325.1:n.915+31T= | |
| NM_002292.3:c.915+31T= | NP_002283.3:n.915+31T= | |
| XM_005265127.3:c.915+31T= | XP_005265184.1:n.915+31T= | |
| XM_005265127.4:c.915+31T= | XP_005265184.1:n.915+31T= | |
| NM_002292.4:c.915+31T= MANE Select | NP_002283.3:n.915+31T= |