Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.66211338C= , CM000674.2:g.66211338C= | GRCh38 |
| NC_000012.11:g.66605118C= , CM000674.1:g.66605118C= | GRCh37 |
| NC_000012.10:g.64891385C= | NCBI36 |
| NG_021194.1:g.27141C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261233.9:c.437-108C= MANE Select | ENSP00000261233.4:n.437-108C= | |
| ENST00000261233.8:c.437-108C= | ENSP00000261233.4:n.437-108C= | |
| ENST00000457197.2:c.254-108C= | ENSP00000409852.2:n.254-108C= | |
| NM_001142523.1:c.254-108C= | NP_001135995.1:n.254-108C= | |
| NM_007199.2:c.437-108C= | NP_009130.2:n.437-108C= | |
| NM_001142523.2:c.254-108C= | NP_001135995.1:n.254-108C= | |
| NM_007199.3:c.437-108C= MANE Select | NP_009130.2:n.437-108C= |