Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142957751C= , CM000669.2:g.142957751C= | GRCh38 |
| NC_000007.13:g.142654838C= , CM000669.1:g.142654838C= | GRCh37 |
| NC_000007.12:g.142364960C= | NCBI36 |
| NG_007492.1:g.9666G= | |
| NG_007492.2:g.9666G= | |
| NG_007492.3:g.9666G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355265.7:c.672+76G= MANE Select | ENSP00000347409.2:n.672+76G= | |
| ENST00000355265.6:c.672+76G= | ENSP00000347409.2:n.672+76G= | |
| ENST00000476829.5:c.525+553G= | ENSP00000419889.1:n.525+553G= | |
| ENST00000479768.6:n.790+76G= | ||
| ENST00000494148.1:n.271+76G= | ||
| NM_000420.2:c.672+76G= | NP_000411.1:n.672+76G= | |
| XM_005249993.2:c.708+76G= | XP_005250050.1:n.708+76G= | |
| NM_000420.3:c.672+76G= MANE Select | NP_000411.1:n.672+76G= |