Linked Data
gnomAD v4:
12-56041956-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56041956A>C , CM000674.2:g.56041956A>C | GRCh38 |
| NC_000012.11:g.56435740A>C , CM000674.1:g.56435740A>C | GRCh37 |
| NC_000012.10:g.54722007A>C | NCBI36 |
| NG_023201.1:g.5055A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-211A>C | ENSP00000348849.5:n.-211A>C | |
| ENST00000646449.2:c.-211A>C MANE Select | ENSP00000496643.1:n.-211A>C | |
| ENST00000356464.9:c.-211A>C | ENSP00000348849.5:n.-211A>C | |
| ENST00000552361.1:c.-143A>C | ENSP00000450339.1:n.-143A>C | |
| NM_001029.3:c.-211A>C | NP_001020.2:n.-211A>C | |
| NM_001029.5:c.-211A>C MANE Select | NP_001020.2:n.-211A>C | |
| XR_944989.3:n.48T>G | ||
| XR_944990.3:n.48T>G |