Linked Data
gnomAD v4:
5-174724586-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724586C>G , CM000667.2:g.174724586C>G | GRCh38 |
| NC_000005.9:g.174151589C>G , CM000667.1:g.174151589C>G | GRCh37 |
| NC_000005.8:g.174084195C>G | NCBI36 |
| NG_008124.1:g.5015C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.-74C>G MANE Select | ENSP00000239243.5:n.-74C>G | |
| ENST00000239243.6:c.-74C>G | ENSP00000239243.5:n.-74C>G | |
| NM_002449.4:c.-74C>G | NP_002440.2:n.-74C>G | |
| NM_001363626.1:c.-74C>G | NP_001350555.1:n.-74C>G | |
| NM_002449.5:c.-74C>G MANE Select | NP_002440.2:n.-74C>G | |
| NM_001363626.2:c.-74C>G | NP_001350555.1:n.-74C>G |