Linked Data
gnomAD v4:
11-72243784-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72243784T>C , CM000673.2:g.72243784T>C | GRCh38 |
| NC_000011.9:g.71954828T>C , CM000673.1:g.71954828T>C | GRCh37 |
| NC_000011.8:g.71632476T>C | NCBI36 |
| NG_008169.1:g.5393A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298231.5:c.217+4A>G MANE Select | ENSP00000298231.5:n.217+4A>G | |
| ENST00000544057.1:n.85+1796A>G | ||
| NM_005169.3:c.217+4A>G | NP_005160.2:n.217+4A>G | |
| NM_005169.4:c.217+4A>G MANE Select | NP_005160.2:n.217+4A>G |