Linked Data
gnomAD v4:
11-112086858-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112086858C>A , CM000673.2:g.112086858C>A | GRCh38 |
| NC_000011.9:g.111957582C>A , CM000673.1:g.111957582C>A | GRCh37 |
| NC_000011.8:g.111462792C>A | NCBI36 |
| NG_012337.2:g.5012C>A | |
| NG_033145.1:g.4941G>T | |
| NG_012337.3:g.5012C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000640554.1:c.-50C>A | ENSP00000491141.1:n.-50C>A | |
| ENST00000375549.7:c.-50C>A | ENSP00000364699.3:n.-50C>A | |
| ENST00000614349.4:c.-50C>A | ENSP00000480666.1:n.-50C>A | |
| NM_001276503.1:c.-50C>A | NP_001263432.1:n.-50C>A | |
| NM_001276504.1:c.-50C>A | NP_001263433.1:n.-50C>A | |
| NM_001276506.1:c.-50C>A | NP_001263435.1:n.-50C>A | |
| NM_003002.3:c.-50C>A | NP_002993.1:n.-50C>A | |
| NR_077060.1:n.35C>A |