Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046237C>A , CM000667.2:g.136046237C>A | GRCh38 |
| NC_000005.9:g.135381926C>A , CM000667.1:g.135381926C>A | GRCh37 |
| NC_000005.8:g.135409825C>A | NCBI36 |
| NG_012646.1:g.22343C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.299-98C>A MANE Select | ENSP00000416330.2:n.299-98C>A | |
| ENST00000442011.6:c.299-98C>A | ENSP00000416330.2:n.299-98C>A | |
| ENST00000504185.5:n.456-98C>A | ||
| ENST00000506699.5:n.364-98C>A | ||
| ENST00000507018.5:c.216-98C>A | ||
| ENST00000515433.1:n.493C>A | ||
| NM_000358.2:c.299-98C>A | NP_000349.1:n.299-98C>A | |
| NM_000358.3:c.299-98C>A MANE Select | NP_000349.1:n.299-98C>A |