Canonical Allele Identifier:
CA2000590022
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164839C= , CM000673.2:g.112164839C= | GRCh38 |
| NC_000011.9:g.112035562C= , CM000673.1:g.112035562C= | GRCh37 |
| NC_000011.8:g.111540772C= | NCBI36 |
| NG_028143.1:g.4279G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525987.5:n.320-5580C= | ||
| ENST00000531744.5:c.315-5580C= | ENSP00000456957.1:n.315-5580C= | |
| ENST00000532699.1:c.315-5580C= | ENSP00000456434.1:n.315-5580C= |