Linked Data
gnomAD v4:
11-61865701-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61865701C>A , CM000673.2:g.61865701C>A | GRCh38 |
| NC_000011.9:g.61633173C>A , CM000673.1:g.61633173C>A | GRCh37 |
| NC_000011.8:g.61389749C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278840.9:c.*12C>A MANE Select | ENSP00000278840.4:n.*12C>A | |
| ENST00000257261.10:c.*12C>A | ENSP00000257261.6:n.*12C>A | |
| ENST00000278840.8:c.*12C>A | ENSP00000278840.4:n.*12C>A | |
| ENST00000522056.5:c.*12C>A | ENSP00000429500.1:n.*12C>A | |
| ENST00000523235.5:n.3427C>A | ||
| NM_001281501.1:c.*12C>A | NP_001268430.1:n.*12C>A | |
| NM_001281502.1:c.*12C>A | NP_001268431.1:n.*12C>A | |
| NM_004265.3:c.*12C>A | NP_004256.1:n.*12C>A | |
| NM_004265.4:c.*12C>A MANE Select | NP_004256.1:n.*12C>A |