Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.2274855C= , CM000681.2:g.2274855C= | GRCh38 |
| NC_000019.9:g.2274854C= , CM000681.1:g.2274854C= | GRCh37 |
| NC_000019.8:g.2225854C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342063.5:c.*825G= MANE Select | ENSP00000345102.3:n.*825G= | |
| ENST00000342063.4:c.*825G= | ENSP00000345102.3:n.*825G= | |
| ENST00000621615.1:c.146+5111C= | ENSP00000481965.1:n.146+5111C= | |
| NM_198532.2:c.*825G= | NP_940934.1:n.*825G= | |
| NM_198532.3:c.*825G= MANE Select | NP_940934.1:n.*825G= |